A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948011



Internal ID18594857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52410958..52414225hg38UCSC Ensembl
Innerchr10:54170718..54173985hg19UCSC Ensembl
Innerchr10:53840724..53843991hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg383268
hg193268
hg183268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1851789, nssv1851796, nssv1851792, nssv1851791, nssv1851793, nssv1851790, nssv1851794, nssv1851797, nssv1851795, nssv1851798
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)nsv948011
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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