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dbVar

Database of genomic structural variation

nsv476998

Organism: Homo sapiens

Study:nstd35 (Kidd et al. 2010)
Variant Type:complex substitution
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:887

Description:complex allele - no allele length provided
Publication(s):Kidd et al. 2010

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: 98 SVs from 31 studies. See in: genome view

Remapped(Score: Perfect):60,048,668-60,049,554

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv476998	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	60,048,668	60,049,554
nsv476998	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	59,816,141	59,817,027
nsv476998	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000011.8	Chr11	59,572,717	59,573,603

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3011233	complex substitution	NA12878	Sequencing	Sequence alignment	1,446

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3011233	Remapped	Perfect	GRCh38.p12	First Pass	NC_000011.10	Chr11	60,048,668	60,049,554
nssv3011233	Remapped	Perfect	GRCh37.p13	First Pass	NC_000011.9	Chr11	59,816,141	59,817,027
nssv3011233	Submitted genomic		NCBI36 (hg18)		NC_000011.8	Chr11	59,572,717	59,573,603

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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