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dbVar

Database of genomic structural variation

esv4334

Organism: Homo sapiens

Study:estd3 (Wang et al. 2008)
Variant Type:sequence alteration
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,681

Publication(s):Wang 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: 193 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):194,822,921-194,825,601

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
esv4334	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	194,822,921	194,825,601
esv4334	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	194,543,650	194,546,330
esv4334	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000003.10	Chr3	196,024,939	196,027,619

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv26775	sequence alteration	YH	Sequencing	Read depth and paired-end mapping	2,682

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
essv26775	Remapped	Perfect	GRCh38.p12	First Pass	NC_000003.12	Chr3	194,822,921	194,825,601
essv26775	Remapped	Perfect	GRCh37.p13	First Pass	NC_000003.11	Chr3	194,543,650	194,546,330
essv26775	Submitted genomic		NCBI36 (hg18)		NC_000003.10	Chr3	196,024,939	196,027,619

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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