A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984096



Internal ID18619286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79663072..79670327hg38UCSC Ensembl
Innerchr15:79955414..79962669hg19UCSC Ensembl
Innerchr15:77742469..77749724hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg387256
hg197256
hg187256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2033108, nssv2033106, nssv2033099, nssv2033104, nssv2033105, nssv2033102, nssv2033101, nssv2033107, nssv2033103, nssv2033100
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)nsv984096
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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