A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968599



Internal ID18257141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21166048..21239961hg38UCSC Ensembl
Innerchr9:21166047..21239960hg19UCSC Ensembl
Innerchr9:21156047..21229960hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3873914
hg1973914
hg1873914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2522772, nssv2522770, nssv2522763, nssv2522771, nssv2522767, nssv2522764, nssv2522768, nssv2522769, nssv2522765, nssv2522766
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIFNA10, IFNA14, IFNA16, IFNA17, IFNA21, IFNA4, IFNA7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968599
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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