A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432222



Internal ID21089775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122173870..122211470hg38UCSC Ensembl
chr8:123186109..123223709hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3837601
hg1937601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432222
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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