A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968603



Internal ID18603831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21406646..21409788hg38UCSC Ensembl
Innerchr9:21406645..21409787hg19UCSC Ensembl
Innerchr9:21396645..21399787hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg383143
hg193143
hg183143
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2524424, nssv2524427, nssv2524422, nssv2524426, nssv2524430, nssv2524429, nssv2524423, nssv2524431, nssv2524425, nssv2524428
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIFNA8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968603
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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