A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974593



Internal ID18609804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67625736..67630786hg38UCSC Ensembl
Innerchr15:67918074..67923124hg19UCSC Ensembl
Innerchr15:65705128..65710178hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385051
hg195051
hg185051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2029694, nssv2029701, nssv2029693, nssv2029698, nssv2029695, nssv2029699, nssv2029702, nssv2029700, nssv2029697, nssv2029696
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMAP2K5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974593
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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