A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081059



Internal ID20648099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173736413..173741177hg38UCSC Ensembl
chr2:174601141..174605905hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg384765
hg194765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351748
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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