A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966260



Internal ID18601490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33825492..33826910hg38UCSC Ensembl
Innerchr4:33827114..33828532hg19UCSC Ensembl
Innerchr4:33503509..33504927hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381419
hg191419
hg181419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2313953, nssv2313949, nssv2313950, nssv2313947, nssv2313945, nssv2313952, nssv2313948, nssv2313944, nssv2313946, nssv2313951
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)nsv966260
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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