A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984081



Internal ID18619271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59965870..59966599hg38UCSC Ensembl
Innerchr15:60258069..60258798hg19UCSC Ensembl
Innerchr15:58045361..58046090hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38730
hg19730
hg18730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028328, nssv2028322, nssv2028329, nssv2028323, nssv2028326, nssv2028330, nssv2028324, nssv2028327, nssv2028325, nssv2028321
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)nsv984081
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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