A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975684



Internal ID18610891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45694788..45698979hg38UCSC Ensembl
Innerchr10:46190236..46194427hg19UCSC Ensembl
Innerchr10:45510242..45514433hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384192
hg194192
hg184192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2611309, nssv2611307, nssv2611308, nssv2611306, nssv2611304, nssv2611303, nssv2611302, nssv2611305, nssv2611301, nssv2611300
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975684
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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