A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966890



Internal ID18602119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135659747..135662862hg38UCSC Ensembl
Innerchr7:135344495..135347610hg19UCSC Ensembl
Innerchr7:134995035..134998150hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg383116
hg193116
hg183116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2479903, nssv2479905, nssv2479901, nssv2479900, nssv2479898, nssv2479896, nssv2479902, nssv2479899, nssv2479904, nssv2479897
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC7orf73
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966890
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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