A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962205



Internal ID16256161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37940970..37943418hg38UCSC Ensembl
Innerchr3:37982461..37984909hg19UCSC Ensembl
Innerchr3:37957465..37959913hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382449
hg192449
hg182449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590079
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)nssv962205
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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