A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980645



Internal ID18615845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58161190..58163586hg38UCSC Ensembl
Innerchr5:57457017..57459413hg19UCSC Ensembl
Innerchr5:57492774..57495170hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382397
hg192397
hg182397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2358484, nssv2358477, nssv2358475, nssv2358480, nssv2358483, nssv2358476, nssv2358481, nssv2358482, nssv2358478, nssv2358479
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)nsv980645
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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