A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv977134



Internal ID15924404
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 StatusS
Merged Variantsnsv592125
Supporting Variants
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)nssv977134
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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