A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963328



Internal ID18598569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73110640..73112351hg38UCSC Ensembl
Innerchr3:73159791..73161502hg19UCSC Ensembl
Innerchr3:73242481..73244192hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381712
hg191712
hg181712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2285246, nssv2285247, nssv2285250, nssv2285251, nssv2285249, nssv2285248, nssv2285245, nssv2285243, nssv2285244, nssv2285242
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963328
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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