A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981517



Internal ID18270028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68240415..68244251hg38UCSC Ensembl
Innerchr7:67705402..67709238hg19UCSC Ensembl
Innerchr7:67342858..67346774hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg383837
hg193837
hg183917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2462481, nssv2462482, nssv2462479, nssv2462478, nssv2462475, nssv2462474, nssv2462477, nssv2462483, nssv2462476, nssv2462480
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)nsv981517
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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