A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948044



Internal ID18594890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67863039..67876307hg38UCSC Ensembl
Innerchr10:69622797..69636065hg19UCSC Ensembl
Innerchr10:69292803..69306071hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813269
hg1913269
hg1813269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1851686, nssv1851684, nssv1851688, nssv1851685, nssv1851690, nssv1851689, nssv1851691, nssv1851682, nssv1851687, nssv1851683
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948044
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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