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dbVar

Database of genomic structural variation

esv2232855

Organism: Homo sapiens

Study:estd194 (Bentley et al. 2008)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:11,309

Publication(s):Bentley et al. 2008

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 240 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):10,516,953-10,528,261

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
esv2232855	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	10,516,953	10,517,021	10,528,212	10,528,261
esv2232855	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	10,556,580	10,556,648	10,567,839	10,567,888
esv2232855	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000007.12	Chr7	10,523,105	10,523,173	10,534,364	10,534,413

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv4913500	deletion	NA18507	Sequencing	Paired-end mapping	504,912

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
essv4913500	Remapped	Perfect	NC_000007.14:g.(10 516953_10517021)_( 10528212_10528261) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	10,516,953	10,517,021	10,528,212	10,528,261
essv4913500	Remapped	Perfect	NC_000007.13:g.(10 556580_10556648)_( 10567839_10567888) del	GRCh37.p13	First Pass	NC_000007.13	Chr7	10,556,580	10,556,648	10,567,839	10,567,888
essv4913500	Submitted genomic		NC_000007.12:g.(10 523105_10523173)_( 10534364_10534413) del	NCBI36 (hg18)		NC_000007.12	Chr7	10,523,105	10,523,173	10,534,364	10,534,413

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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