A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974619



Internal ID18609830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92281681..92288740hg38UCSC Ensembl
Innerchr15:92824911..92831970hg19UCSC Ensembl
Innerchr15:90625915..90632974hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387060
hg197060
hg187060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2037745, nssv2037744, nssv2037741, nssv2037743, nssv2037748, nssv2037742, nssv2037746, nssv2037747, nssv2037750, nssv2037749
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)nsv974619
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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