A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968657



Internal ID18603885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62098441..62100018hg38UCSC Ensembl
Innerchr9:45234593..45236170hg19UCSC Ensembl
Innerchr9:45174589..45176166hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381578
hg191578
hg181578
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2542261, nssv2542264, nssv2542260, nssv2542265, nssv2542263, nssv2542262, nssv2541466, nssv2541465, nssv2542266, nssv2541467
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)nsv968657
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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