A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131776



Internal ID20698816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55894587..55897015hg38UCSC Ensembl
chr5:55190415..55192843hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408713
Supporting Variants
Samples
Known GenesIL31RA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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