A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670835



Internal ID15407487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24152472..24188295hg38UCSC Ensembl
Innerchr15:24397619..24433442hg19UCSC Ensembl
Innerchr15:21948712..21984535hg18UCSC Ensembl
Innerchr15:21948712..21984535hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3835824
hg1935824
hg1835824
hg1735824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv670835
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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