A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974549



Internal ID18609760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30891480..30900857hg38UCSC Ensembl
Innerchr15:31183683..31193060hg19UCSC Ensembl
Innerchr15:28970975..28980352hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg389378
hg199378
hg189378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2015957, nssv2015962, nssv2015958, nssv2015961, nssv2015953, nssv2015959, nssv2015955, nssv2015954, nssv2015956, nssv2015960
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)nsv974549
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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