A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335941



Internal ID20993494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27572611..27573115hg38UCSC Ensembl
chr2:27795478..27795982hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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