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dbVar

Database of genomic structural variation

nsv474990

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:85

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: 99 SVs from 28 studies. See in: genome view

Remapped(Score: Perfect):49,489,776-49,489,860

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv474990	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	49,489,776	49,489,860
nsv474990	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000014.7	Chr14	48,559,526	48,559,610

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3019885	complex substitution	NA18956	Sequencing	Sequence alignment	601

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3019885	Remapped	Perfect	GRCh37.p13	First Pass	NC_000014.8	Chr14	49,489,776	49,489,860
nssv3019885	Submitted genomic		NCBI36 (hg18)		NC_000014.7	Chr14	48,559,526	48,559,610

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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