A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976925



Internal ID18612131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41716908..41723066hg38UCSC Ensembl
Innerchr15:42009106..42015264hg19UCSC Ensembl
Innerchr15:39796398..39802556hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386159
hg196159
hg186159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2019259, nssv2019260, nssv2019265, nssv2019266, nssv2019262, nssv2019264, nssv2019263, nssv2019261, nssv2019258, nssv2019257
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMGA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976925
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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