A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962148



Internal ID16256104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37935209..37945349hg38UCSC Ensembl
Innerchr3:37976700..37986840hg19UCSC Ensembl
Innerchr3:37951704..37961844hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3810141
hg1910141
hg1810141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590069
Supporting Variants
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962148
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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