A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693812



Internal ID15430464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158549149..158551602hg38UCSC Ensembl
Innerchr1:158518939..158521392hg19UCSC Ensembl
Innerchr1:156785563..156788016hg18UCSC Ensembl
Innerchr1:155332012..155334465hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382454
hg192454
hg182454
hg172454
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515774
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693812
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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