A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974597



Internal ID18609808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74046885..74121313hg38UCSC Ensembl
Innerchr15:74339226..74413654hg19UCSC Ensembl
Innerchr15:72126279..72200707hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3874429
hg1974429
hg1874429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2030686, nssv2030679, nssv2030683, nssv2030682, nssv2030687, nssv2030680, nssv2030684, nssv2030681, nssv2030688, nssv2030685
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGOLGA6A, PML
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974597
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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