A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673946



Internal ID15410598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24131475..24183151hg38UCSC Ensembl
Innerchr15:24376622..24428298hg19UCSC Ensembl
Innerchr15:21927715..21979391hg18UCSC Ensembl
Innerchr15:21927715..21979391hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3851677
hg1951677
hg1851677
hg1751677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known GenesPWRN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673946
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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