A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971767



Internal ID18606984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133768944..133772058hg38UCSC Ensembl
Innerchr10:135506269..135509383hg19UCSC Ensembl
Innerchr10:135356259..135359373hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383115
hg193115
hg183115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2616646, nssv2616641, nssv2616644, nssv2616648, nssv2616647, nssv2616639, nssv2616640, nssv2616643, nssv2616645, nssv2616642
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971767
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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