A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945761



Internal ID18592612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8785164..8789641hg38UCSC Ensembl
Innerchr1:8845223..8849700hg19UCSC Ensembl
Innerchr1:8767810..8772287hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg384478
hg194478
hg184478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1752708, nssv1752704, nssv1752713, nssv1752705, nssv1752712, nssv1752707, nssv1752711, nssv1752706, nssv1752710, nssv1752709
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRERE
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945761
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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