A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339434



Internal ID20996987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168449722..168451949hg38UCSC Ensembl
chr2:169306232..169308459hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382228
hg192228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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