A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151775



Internal ID15532505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:51370620..51466575hg38UCSC Ensembl
Innerchr3:51408051..51500591hg19UCSC Ensembl
Innerchr3:51383091..51475631hg18UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3895956
hg1992541
hg1892541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590277
Supporting Variants
SamplesHGDP01324
Known GenesDOCK3, MANF, RBM15B, VPRBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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