A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948045



Internal ID18248205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67960788..67961380hg38UCSC Ensembl
Innerchr10:69720545..69721137hg19UCSC Ensembl
Innerchr10:69390551..69391143hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38593
hg19593
hg18593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1852844, nssv1852840, nssv1852843, nssv1852848, nssv1852842, nssv1852839, nssv1852841, nssv1852847, nssv1852845, nssv1852846
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948045
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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