A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984103



Internal ID18619293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83195045..83195665hg38UCSC Ensembl
Innerchr15:83863797..83864417hg19UCSC Ensembl
Innerchr15:81654801..81655421hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38621
hg19621
hg18621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2034835, nssv2034836, nssv2034840, nssv2034841, nssv2034838, nssv2034833, nssv2034834, nssv2034842, nssv2034839, nssv2034837
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHDGFRP3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984103
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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