A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152536



Internal ID15875371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119015424..119090661hg38UCSC Ensembl
Innerchr3:118734271..118809508hg19UCSC Ensembl
Innerchr3:120216961..120292198hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3875238
hg1975238
hg1875238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591358
Supporting Variants
SamplesHGDP00675
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152536
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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