A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006674



Internal ID19095892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:78422910..78442260hg38UCSC Ensembl
Innerchr3:78472060..78491410hg19UCSC Ensembl
Innerchr3:78554750..78574100hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3819351
hg1919351
hg1819351
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596222, nssv3596220, nssv3596221
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)nsv1006674
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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