A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132957



Internal ID20699997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8212831..8222354hg38UCSC Ensembl
chr5:8212944..8222467hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg389524
hg199524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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