A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966245



Internal ID18601475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:381227..393695hg38UCSC Ensembl
Innerchr4:375016..387484hg19UCSC Ensembl
Innerchr4:365016..377484hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3812469
hg1912469
hg1812469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2309307, nssv2309310, nssv2309313, nssv2309315, nssv2309309, nssv2309312, nssv2309308, nssv2309311, nssv2309306, nssv2309314
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)nsv966245
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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