A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968622



Internal ID18603850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39412910..39440246hg38UCSC Ensembl
Innerchr9:39412907..39440245hg19UCSC Ensembl
Innerchr9:39402907..39430245hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3827337
hg1927339
hg1827339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2532381, nssv2532388, nssv2532383, nssv2532386, nssv2532384, nssv2532382, nssv2532380, nssv2532389, nssv2532385, nssv2532387
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)nsv968622
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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