A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131772



Internal ID20698812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55782422..55785607hg38UCSC Ensembl
chr5:55078250..55081435hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg383186
hg193186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396101
Supporting Variants
Samples
Known GenesDDX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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