A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662314



Internal ID15398966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37513008..37544959hg38UCSC Ensembl
Innerchr13:38087145..38119096hg19UCSC Ensembl
Innerchr13:36985145..37017096hg18UCSC Ensembl
Innerchr13:36985145..37017096hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3831952
hg1931952
hg1831952
hg1731952
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517476
Supporting Variants
Samples
Known GenesLINC00547
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662314
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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