A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337896



Internal ID20995449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183854255..183871126hg38UCSC Ensembl
chr2:184718982..184735853hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3816872
hg1916872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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