A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982203



Internal ID18270712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21438415..21441585hg38UCSC Ensembl
Innerchr9:21438414..21441584hg19UCSC Ensembl
Innerchr9:21428414..21431584hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg383171
hg193171
hg183171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2524619, nssv2524616, nssv2524625, nssv2524617, nssv2524621, nssv2524623, nssv2524618, nssv2524624, nssv2524620, nssv2524622
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIFNA1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982203
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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