A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984056



Internal ID18619246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41163385..41165495hg38UCSC Ensembl
Innerchr15:41455583..41457693hg19UCSC Ensembl
Innerchr15:39242875..39244985hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382111
hg192111
hg182111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2020448, nssv2020447, nssv2020449, nssv2020446, nssv2020452, nssv2020445, nssv2020444, nssv2020451, nssv2020443, nssv2020450
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)nsv984056
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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