A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591350



Internal ID16378759
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 StatusM
Merged Variants
Supporting Variantsnssv971640
Samples
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591350
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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