A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967769



Internal ID18602997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85246389..85249103hg38UCSC Ensembl
Innerchr4:86167542..86170256hg19UCSC Ensembl
Innerchr4:86386566..86389280hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg382715
hg192715
hg182715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2325403, nssv2325398, nssv2325407, nssv2325404, nssv2325399, nssv2325402, nssv2325405, nssv2325406, nssv2325400, nssv2325401
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)nsv967769
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