A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345941



Internal ID21003494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38338377..38345513hg38UCSC Ensembl
chr2:38565519..38572655hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg387137
hg197137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087791
Samples
Known GenesATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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