A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980270



Internal ID18615470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164260118..164280806hg38UCSC Ensembl
Innerchr4:165181270..165201958hg19UCSC Ensembl
Innerchr4:165400720..165421408hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3820689
hg1920689
hg1820689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2339216, nssv2339219, nssv2339218, nssv2339214, nssv2339222, nssv2339217, nssv2339221, nssv2339223, nssv2339215, nssv2339220
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMARCH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980270
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