A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966873



Internal ID18602102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103158058..103164911hg38UCSC Ensembl
Innerchr7:102798505..102805358hg19UCSC Ensembl
Innerchr7:102585741..102592594hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386854
hg196854
hg186854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2472259, nssv2472251, nssv2472257, nssv2472256, nssv2472253, nssv2472255, nssv2472254, nssv2472252, nssv2472258, nssv2472250
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)nsv966873
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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