A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133082



Internal ID20700122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85783580..85790907hg38UCSC Ensembl
chr5:85079398..85086725hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg387328
hg197328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399182
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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