A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966805



Internal ID18602035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61071607..61074642hg38UCSC Ensembl
Innerchr7:61054332..61057367hg19UCSC Ensembl
Innerchr7:61058085..61061309hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg383036
hg193036
hg183225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv76n82
Supporting Variantsnssv2451846, nssv2451840, nssv2451844, nssv2451843, nssv2451848, nssv2451847, nssv2451845, nssv2451839, nssv2451842, nssv2451841
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)nsv966805
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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