A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966833



Internal ID18602063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66452512..66467093hg38UCSC Ensembl
Innerchr7:65917499..65932080hg19UCSC Ensembl
Innerchr7:65554934..65569515hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3814582
hg1914582
hg1814582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2458982, nssv2458980, nssv2458984, nssv2458975, nssv2458976, nssv2458981, nssv2458983, nssv2458978, nssv2458977, nssv2458979
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)nsv966833
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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