A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686510



Internal ID15423162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155687239..155706412hg38UCSC Ensembl
Innerchr6:156008373..156027546hg19UCSC Ensembl
Innerchr6:156050065..156069238hg18UCSC Ensembl
Innerchr6:156100486..156119659hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3819174
hg1919174
hg1819174
hg1719174
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686510
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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