A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344986



Internal ID21002539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160230294..160233240hg38UCSC Ensembl
chr2:161086805..161089751hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382947
hg192947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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