A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982540



Internal ID18617735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68285669..68298799hg38UCSC Ensembl
Innerchr9:70900585..70913715hg19UCSC Ensembl
Innerchr9:70090405..70103535hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3813131
hg1913131
hg1813131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2749734, nssv2748351, nssv2756562, nssv2755770, nssv2755140, nssv2751521, nssv2753930, nssv2749366, nssv2750573, nssv2754170
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982540
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer