A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132104



Internal ID20699144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64694397..64697118hg38UCSC Ensembl
chr5:63990224..63992945hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382722
hg192722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407394
Supporting Variants
Samples
Known GenesFAM159B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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