A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982212



Internal ID18617407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35942094..35943917hg38UCSC Ensembl
Innerchr9:35942091..35943914hg19UCSC Ensembl
Innerchr9:35932091..35933914hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381824
hg191824
hg181824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527940, nssv2527941, nssv2527943, nssv2527945, nssv2527936, nssv2527937, nssv2527942, nssv2527944, nssv2527938, nssv2527939
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982212
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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