A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974928



Internal ID18610137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45824376..45833168hg38UCSC Ensembl
Innerchr10:46319824..46328616hg19UCSC Ensembl
Innerchr10:45639830..45648622hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388793
hg198793
hg188793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2612390, nssv2612391, nssv2612396, nssv2612395, nssv2612388, nssv2612392, nssv2612389, nssv2612393, nssv2612387, nssv2612394
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974928
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