A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698046



Internal ID15434698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37169903..37218318hg38UCSC Ensembl
Innerchr1:37635504..37683919hg19UCSC Ensembl
Innerchr1:37408091..37456506hg18UCSC Ensembl
Innerchr1:37304597..37353012hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3848416
hg1948416
hg1848416
hg1748416
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521436
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698046
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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