A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518097



Internal ID15098704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58667074..58672732hg38UCSC Ensembl
Innerchr15:58959273..58964931hg19UCSC Ensembl
Innerchr15:56746565..56752223hg18UCSC Ensembl
Innerchr15:56746565..56752223hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385659
hg195659
hg185659
hg175659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695510
Samples
Known GenesADAM10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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