A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972458



Internal ID18607674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132370615..132375403hg38UCSC Ensembl
Innerchr9:135246002..135250790hg19UCSC Ensembl
Innerchr9:134235823..134240611hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384789
hg194789
hg184789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2566741, nssv2566749, nssv2566747, nssv2566750, nssv2566743, nssv2566746, nssv2566744, nssv2566745, nssv2566742, nssv2566748
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)nsv972458
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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