A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149190



Internal ID15874696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24059521..24240013hg38UCSC Ensembl
Innerchr15:24304668..24485160hg19UCSC Ensembl
Innerchr15:21855761..22036253hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38180493
hg19180493
hg18180493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568378
Supporting Variants
SamplesHGDP00574
Known GenesPWRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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