A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710757



Internal ID18662352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119722279..119759932hg38UCSC Ensembl
Innerchr11:119592989..119630641hg19UCSC Ensembl
Innerchr11:119098199..119135851hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3837654
hg1937653
hg1837653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037739
Supporting Variants
Samples
Known GenesPVRL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710757
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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