A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972650



Internal ID18607866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14069159..14070793hg38UCSC Ensembl
Innerchr9:14069158..14070792hg19UCSC Ensembl
Innerchr9:14059158..14060792hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381635
hg191635
hg181635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2522173, nssv2522175, nssv2522172, nssv2522177, nssv2522178, nssv2522179, nssv2522180, nssv2522174, nssv2522171, nssv2522176
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)nsv972650
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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