A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342662



Internal ID21000215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163461483..163464114hg38UCSC Ensembl
chr2:164317993..164320624hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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