A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967819



Internal ID18603047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184296683..184300613hg38UCSC Ensembl
Innerchr4:185217836..185221766hg19UCSC Ensembl
Innerchr4:185454830..185458760hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg383931
hg193931
hg183931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2343016, nssv2343008, nssv2343017, nssv2343012, nssv2343015, nssv2343010, nssv2343009, nssv2343014, nssv2343011, nssv2343013
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)nsv967819
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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