A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968602



Internal ID18603830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21349790..21352301hg38UCSC Ensembl
Innerchr9:21349789..21352300hg19UCSC Ensembl
Innerchr9:21339789..21342300hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382512
hg192512
hg182512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2524908, nssv2524903, nssv2524905, nssv2524907, nssv2524910, nssv2524911, nssv2524909, nssv2524902, nssv2524906, nssv2524904
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIFNA6
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968602
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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