A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211144



Internal ID20778184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161740601..161826700hg38UCSC Ensembl
chr4:162661753..162747852hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3886100
hg1986100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388390
Supporting Variants
Samples
Known GenesFSTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211144
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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