A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966832



Internal ID18602062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66436947..66451041hg38UCSC Ensembl
Innerchr7:65901934..65916028hg19UCSC Ensembl
Innerchr7:65539369..65553463hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3814095
hg1914095
hg1814095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2458881, nssv2458886, nssv2458883, nssv2458884, nssv2458882, nssv2458878, nssv2458887, nssv2458879, nssv2458885, nssv2458880
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)nsv966832
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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