A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009500



Internal ID19098718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6262764..6293773hg38UCSC Ensembl
Innerchr3:6304451..6335460hg19UCSC Ensembl
Innerchr3:6279451..6310460hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3831010
hg1931010
hg1831010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4671n100
Supporting Variantsnssv3591815
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)nsv1009500
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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