A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971640



Internal ID16265596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119000633..119104294hg38UCSC Ensembl
Innerchr3:118719480..118823141hg19UCSC Ensembl
Innerchr3:120202170..120305831hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38103662
hg19103662
hg18103662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591350
Supporting Variants
Samples
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv971640
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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