A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966760



Internal ID18601990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20843410..20844156hg38UCSC Ensembl
Innerchr7:20883029..20883775hg19UCSC Ensembl
Innerchr7:20849554..20850300hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38747
hg19747
hg18747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438055, nssv2438054, nssv2438052, nssv2438051, nssv2438048, nssv2438047, nssv2438049, nssv2438046, nssv2438050, nssv2438053
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)nsv966760
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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