A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591404



Internal ID16032127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122181001..122216979hg38UCSC Ensembl
Innerchr3:121899848..121935826hg19UCSC Ensembl
Innerchr3:123382538..123418516hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3835979
hg1935979
hg1835979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8526n54
Supporting Variantsnssv971769
Samples
Known GenesCASR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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