A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984109



Internal ID18619299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91034903..91041439hg38UCSC Ensembl
Innerchr15:91578133..91584669hg19UCSC Ensembl
Innerchr15:89379137..89385673hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386537
hg196537
hg186537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2037652, nssv2037646, nssv2037650, nssv2037649, nssv2037648, nssv2037644, nssv2037647, nssv2037651, nssv2037653, nssv2037645
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)nsv984109
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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