A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592125



Internal ID16032848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158887176..159093279hg38UCSC Ensembl
Innerchr3:158604965..158811068hg19UCSC Ensembl
Innerchr3:160087659..160293762hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38206104
hg19206104
hg18206104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv977134
Samples
Known GenesIQCJ, IQCJ-SCHIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592125
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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