A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355529



Internal ID21013082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240152150..240183644hg38UCSC Ensembl
chr2:241091567..241123061hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3831495
hg1931495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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