A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972367



Internal ID18607583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62454535..62457730hg38UCSC Ensembl
Innerchr9:46765836..46769031hg19UCSC Ensembl
Innerchr9:46605832..46609027hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383196
hg193196
hg183196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2543493, nssv2543489, nssv2543485, nssv2543486, nssv2543494, nssv2543490, nssv2543492, nssv2543487, nssv2543488, nssv2543491
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)nsv972367
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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