A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984077



Internal ID18619267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59045777..59051886hg38UCSC Ensembl
Innerchr15:59337976..59344085hg19UCSC Ensembl
Innerchr15:57125268..57131377hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg386110
hg196110
hg186110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2025271, nssv2025273, nssv2025265, nssv2025268, nssv2025269, nssv2025272, nssv2025264, nssv2025266, nssv2025267, nssv2025270
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRNF111
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984077
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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