A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998614



Internal ID18811464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2760022..2816534hg38UCSC Ensembl
Innerchr3:2801706..2858218hg19UCSC Ensembl
Innerchr3:2776706..2833218hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3856513
hg1956513
hg1856513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590376
Samples
Known GenesCNTN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998614
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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