A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083871



Internal ID20650911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191439914..191442521hg38UCSC Ensembl
chr2:192304640..192307247hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg382608
hg192608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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