A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700266



Internal ID15436918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24152415..24287455hg38UCSC Ensembl
Innerchr15:24397562..24532602hg19UCSC Ensembl
Innerchr15:21948655..22083695hg18UCSC Ensembl
Innerchr15:21948655..22083695hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38135041
hg19135041
hg18135041
hg17135041
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)nssv700266
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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