A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972401



Internal ID18607617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74934909..74935645hg38UCSC Ensembl
Innerchr9:77549825..77550561hg19UCSC Ensembl
Innerchr9:76739645..76740381hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38737
hg19737
hg18737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2553389, nssv2553392, nssv2553390, nssv2553385, nssv2553386, nssv2553388, nssv2553387, nssv2553393, nssv2553391, nssv2553394
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)nsv972401
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