A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970573



Internal ID18605795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113494544..113500253hg38UCSC Ensembl
Innerchr7:113134599..113140308hg19UCSC Ensembl
Innerchr7:112921835..112927544hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg385710
hg195710
hg185710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2475726, nssv2475718, nssv2475723, nssv2475719, nssv2475724, nssv2475722, nssv2475720, nssv2475725, nssv2475721, nssv2475717
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)nsv970573
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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