A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982208



Internal ID18617403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33516499..33614298hg38UCSC Ensembl
Innerchr9:33516497..33614296hg19UCSC Ensembl
Innerchr9:33506497..33604296hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3897800
hg1997800
hg1897800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2526636, nssv2526643, nssv2526639, nssv2526637, nssv2526635, nssv2526644, nssv2526640, nssv2526638, nssv2526641, nssv2526642
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD18B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982208
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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