A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152487



Internal ID15528508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:67343205..67662546hg38UCSC Ensembl
Innerchr3:67393629..67712970hg19UCSC Ensembl
Innerchr3:67476319..67795660hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38319342
hg19319342
hg18319342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590560
Supporting Variants
SamplesHGDP00649
Known GenesSUCLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152487
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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