A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv975220



Internal ID15922490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143043645..143122898hg38UCSC Ensembl
Innerchr3:142762487..142841740hg19UCSC Ensembl
Innerchr3:144245177..144324430hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3879254
hg1979254
hg1879254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591921
Supporting Variants
Samples
Known GenesCHST2, U2SURP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv975220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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