A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948203



Internal ID18595049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118928321..118933098hg38UCSC Ensembl
Innerchr10:120687833..120692610hg19UCSC Ensembl
Innerchr10:120677823..120682600hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384778
hg194778
hg184778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868650, nssv1868647, nssv1868651, nssv1868646, nssv1868648, nssv1868645, nssv1868644, nssv1868649, nssv1868652, nssv1868643
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)nsv948203
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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