A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948042



Internal ID18594888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67750333..67757117hg38UCSC Ensembl
Innerchr10:69510091..69516875hg19UCSC Ensembl
Innerchr10:69180097..69186881hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg386785
hg196785
hg186785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1852227, nssv1852229, nssv1852228, nssv1852225, nssv1852230, nssv1852232, nssv1852226, nssv1852231, nssv1852234, nssv1852233
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)nsv948042
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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