A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694229



Internal ID15430881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76918836..76924565hg38UCSC Ensembl
Innerchr13:77492970..77498699hg19UCSC Ensembl
Innerchr13:76390971..76396700hg18UCSC Ensembl
Innerchr13:76390971..76396700hg17UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg385730
hg195730
hg185730
hg175730
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518365
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694229
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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