A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984091



Internal ID18272595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74348034..74366664hg38UCSC Ensembl
Innerchr15:74640375..74659005hg19UCSC Ensembl
Innerchr15:72427428..72446058hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3818631
hg1918631
hg1818631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2030878, nssv2030879, nssv2030880, nssv2030876, nssv2030875, nssv2030873, nssv2030874, nssv2030881, nssv2030882, nssv2030877
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCYP11A1, LOC729739
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984091
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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