A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967572



Internal ID18602800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26378687..26381162hg38UCSC Ensembl
Innerchr8:26236203..26238678hg19UCSC Ensembl
Innerchr8:26292120..26294595hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg382476
hg192476
hg182476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2497276, nssv2497272, nssv2497274, nssv2497269, nssv2497268, nssv2497277, nssv2497273, nssv2497270, nssv2497271, nssv2497275
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)nsv967572
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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