A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002427



Internal ID18744959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2620880..2722621hg38UCSC Ensembl
Innerchr3:2662564..2764305hg19UCSC Ensembl
Innerchr3:2637564..2739305hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38101742
hg19101742
hg18101742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739546
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)nsv1002427
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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