A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984137



Internal ID18619327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28659180..28664471hg38UCSC Ensembl
Innerchr15:28904326..28909617hg19UCSC Ensembl
Innerchr15:26703367..26708658hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg385292
hg195292
hg185292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2628730, nssv2628734, nssv2628725, nssv2628726, nssv2628732, nssv2628727, nssv2628733, nssv2628728, nssv2628731, nssv2628729
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P9
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984137
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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