A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18130444



Internal ID20697484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36244000..36246018hg38UCSC Ensembl
chr5:36244102..36246120hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382019
hg192019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18130444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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