A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980266



Internal ID18615466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152792844..152796818hg38UCSC Ensembl
Innerchr4:153713996..153717970hg19UCSC Ensembl
Innerchr4:153933446..153937420hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383975
hg193975
hg183975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2338614, nssv2338610, nssv2338608, nssv2338609, nssv2338611, nssv2338612, nssv2338613, nssv2338607, nssv2338615, nssv2338616
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesARFIP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980266
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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