A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948115



Internal ID18594961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87133484..87151391hg38UCSC Ensembl
Innerchr10:88893241..88911148hg19UCSC Ensembl
Innerchr10:88883221..88901128hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3817908
hg1917908
hg1817908
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1863072, nssv1863074, nssv1863071, nssv1863070, nssv1863068, nssv1863073, nssv1863077, nssv1863069, nssv1863076, nssv1863075
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM35A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948115
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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