A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970521



Internal ID18605743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68112832..68121967hg38UCSC Ensembl
Innerchr7:67577819..67586954hg19UCSC Ensembl
Innerchr7:67215254..67224389hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg389136
hg199136
hg189136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2462380, nssv2462382, nssv2462378, nssv2462386, nssv2462384, nssv2462385, nssv2462383, nssv2462381, nssv2462377, nssv2462379
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970521
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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