A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948161



Internal ID18595007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99039952..99051401hg38UCSC Ensembl
Innerchr10:100799709..100811158hg19UCSC Ensembl
Innerchr10:100789699..100801148hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3811450
hg1911450
hg1811450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865155, nssv1865153, nssv1865152, nssv1865151, nssv1865156, nssv1865157, nssv1865154, nssv1865160, nssv1865158, nssv1865159
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHPSE2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948161
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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