A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010701



Internal ID19099918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26513706..26575774hg38UCSC Ensembl
Innerchr3:26555197..26617265hg19UCSC Ensembl
Innerchr3:26530201..26592269hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3862069
hg1962069
hg1862069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4712n100
Supporting Variantsnssv3589557
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010701
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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