A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702269



Internal ID15438921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67865543..67874592hg38UCSC Ensembl
Innerchr15:68157881..68166930hg19UCSC Ensembl
Innerchr15:65944935..65953984hg18UCSC Ensembl
Innerchr15:65944935..65953984hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg389050
hg199050
hg189050
hg179050
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526037
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702269
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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