A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981545



Internal ID18616742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87521465..87524142hg38UCSC Ensembl
Innerchr7:87150781..87153458hg19UCSC Ensembl
Innerchr7:86988717..86991394hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382678
hg192678
hg182678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2467733, nssv2467731, nssv2467736, nssv2467730, nssv2467734, nssv2467737, nssv2467732, nssv2467735, nssv2467738, nssv2467739
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesABCB1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981545
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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