A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694852



Internal ID15431504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24240013..24404104hg38UCSC Ensembl
Innerchr15:24485160..24649251hg19UCSC Ensembl
Innerchr15:22036253..22200344hg18UCSC Ensembl
Innerchr15:22036253..22200344hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38164092
hg19164092
hg18164092
hg17164092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694852
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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