A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011135



Internal ID18753669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116380194..119036472hg38UCSC Ensembl
Innerchr3:116099041..118755319hg19UCSC Ensembl
Innerchr3:117581731..120238009hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg382656279
hg192656279
hg182656279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604482
Samples
Known GenesIGSF11, IGSF11-AS1, LSAMP, TUSC7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011135
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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