A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122696



Internal ID20689736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:104051374..104080471hg38UCSC Ensembl
chr5:103387075..103416172hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3829098
hg1929098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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