A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967806



Internal ID18603034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159006917..159008826hg38UCSC Ensembl
Innerchr4:159928069..159929978hg19UCSC Ensembl
Innerchr4:160147519..160149428hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381910
hg191910
hg181910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2340081, nssv2340083, nssv2340087, nssv2340082, nssv2340089, nssv2340088, nssv2340086, nssv2340080, nssv2340085, nssv2340084
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC4orf45
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967806
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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