A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678772



Internal ID15415424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51978483..52013267hg38UCSC Ensembl
Innerchr15:52270680..52305464hg19UCSC Ensembl
Innerchr15:50057972..50092756hg18UCSC Ensembl
Innerchr15:50057972..50092756hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3834785
hg1934785
hg1834785
hg1734785
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517399
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678772
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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