A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945832



Internal ID18245996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25293460..25294559hg38UCSC Ensembl
Innerchr1:25619951..25621050hg19UCSC Ensembl
Innerchr1:25492538..25493637hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381100
hg191100
hg181100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1764665, nssv1764670, nssv1764663, nssv1764667, nssv1764669, nssv1764671, nssv1764666, nssv1764662, nssv1764664, nssv1764668
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRHD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945832
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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