A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967818



Internal ID18603046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183483817..183484317hg38UCSC Ensembl
Innerchr4:184404970..184405470hg19UCSC Ensembl
Innerchr4:184641964..184642464hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2342917, nssv2342920, nssv2342911, nssv2342916, nssv2342919, nssv2342918, nssv2342914, nssv2342915, nssv2342913, nssv2342912
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)nsv967818
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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