A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673559



Internal ID15410211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24136736..24188801hg38UCSC Ensembl
Innerchr15:24381883..24433948hg19UCSC Ensembl
Innerchr15:21932976..21985041hg18UCSC Ensembl
Innerchr15:21932976..21985041hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3852066
hg1952066
hg1852066
hg1752066
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)nssv673559
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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