A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947764



Internal ID18594611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21101856..21113598hg38UCSC Ensembl
Innerchr10:21390785..21402527hg19UCSC Ensembl
Innerchr10:21430791..21442533hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3811743
hg1911743
hg1811743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1832676, nssv1832672, nssv1832670, nssv1832673, nssv1832669, nssv1832671, nssv1832674, nssv1832678, nssv1832675, nssv1832677
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNEBL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947764
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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