A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948026



Internal ID18248186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58192038..58196638hg38UCSC Ensembl
Innerchr10:59951799..59956399hg19UCSC Ensembl
Innerchr10:59621805..59626405hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384601
hg194601
hg184601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1851260, nssv1851258, nssv1851265, nssv1851264, nssv1851262, nssv1851259, nssv1851263, nssv1851261, nssv1851256, nssv1851257
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIPMK
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948026
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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