A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967624



Internal ID18602852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103084398..103085335hg38UCSC Ensembl
Innerchr8:104096626..104097563hg19UCSC Ensembl
Innerchr8:104165802..104166739hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38938
hg19938
hg18938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2516031, nssv2516028, nssv2516035, nssv2516032, nssv2516026, nssv2516033, nssv2516027, nssv2516030, nssv2516029, nssv2516034
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)nsv967624
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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