A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947946



Internal ID18248106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46238597..46247305hg38UCSC Ensembl
Innerchr10:47609833..47618541hg19UCSC Ensembl
Innerchr10:47079839..47088547hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388709
hg198709
hg188709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1853792, nssv1853798, nssv1853793, nssv1853794, nssv1853801, nssv1853800, nssv1853799, nssv1853795, nssv1853797, nssv1853796
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesANTXRLP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947946
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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