A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948196



Internal ID18595042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:116748475..116752294hg38UCSC Ensembl
Innerchr10:118507986..118511805hg19UCSC Ensembl
Innerchr10:118497976..118501795hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383820
hg193820
hg183820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868210, nssv1868211, nssv1868216, nssv1868212, nssv1868215, nssv1868214, nssv1868208, nssv1868207, nssv1868209, nssv1868213
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)nsv948196
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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