A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151906



Internal ID15532081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62624950..62626338hg38UCSC Ensembl
Innerchr3:62610625..62612013hg19UCSC Ensembl
Innerchr3:62585665..62587053hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381389
hg191389
hg181389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590442
Supporting Variants
SamplesHGDP01255
Known GenesCADPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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