A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947767



Internal ID18594614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22267265..22268772hg38UCSC Ensembl
Innerchr10:22556194..22557701hg19UCSC Ensembl
Innerchr10:22596200..22597707hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381508
hg191508
hg181508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1833805, nssv1833806, nssv1833812, nssv1833808, nssv1833813, nssv1833804, nssv1833811, nssv1833810, nssv1833807, nssv1833809
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)nsv947767
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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