A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966307



Internal ID18601537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109787727..109800543hg38UCSC Ensembl
Innerchr4:110708883..110721699hg19UCSC Ensembl
Innerchr4:110928332..110941148hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3812817
hg1912817
hg1812817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2332030, nssv2332027, nssv2332025, nssv2332024, nssv2332023, nssv2332026, nssv2332031, nssv2332029, nssv2332028, nssv2332022
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCFI
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966307
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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