A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982535



Internal ID18617730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65810137..65830543hg38UCSC Ensembl
Innerchr9:70335502..70355908hg19UCSC Ensembl
Innerchr9:69575322..69595728hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820407
hg1920407
hg1820407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2751332, nssv2749144, nssv2747372, nssv2754995, nssv2753618, nssv2754376, nssv2753392, nssv2753284, nssv2750395, nssv2756263
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982535
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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