A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336896



Internal ID20994449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19483239..19489869hg38UCSC Ensembl
chr2:19683000..19689630hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg386631
hg196631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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