A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998076



Internal ID19157613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142102091..142367817hg38UCSC Ensembl
Innerchr3:141820933..142086659hg19UCSC Ensembl
Innerchr3:143303623..143569349hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38265727
hg19265727
hg18265727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4912n100
Supporting Variantsnssv3741479, nssv3606110, nssv3741481, nssv3741477, nssv3606108, nssv3741480, nssv3606112, nssv3741475, nssv3741473, nssv3606111, nssv3741478, nssv3741476, nssv3606109, nssv3741474
Samples
Known GenesGK5, TFDP2, XRN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998076
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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