A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666817



Internal ID15403469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23187743..23191854hg38UCSC Ensembl
Innerchr13:23761882..23765993hg19UCSC Ensembl
Innerchr13:22659882..22663993hg18UCSC Ensembl
Innerchr13:22659882..22663993hg17UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg384112
hg194112
hg184112
hg174112
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517054
Supporting Variants
Samples
Known GenesSGCG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666817
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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