A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948176



Internal ID18595022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:104156978..104157478hg38UCSC Ensembl
Innerchr10:105916736..105917236hg19UCSC Ensembl
Innerchr10:105906726..105907226hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1864891, nssv1864892, nssv1864890, nssv1864884, nssv1864888, nssv1864885, nssv1864883, nssv1864889, nssv1864886, nssv1864887
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWDR96
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948176
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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