A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347758



Internal ID21005311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216793489..216798411hg38UCSC Ensembl
chr2:217658212..217663134hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg384923
hg194923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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