A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132118



Internal ID20699158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64838092..64838438hg38UCSC Ensembl
chr5:64133919..64134265hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396438
Supporting Variants
Samples
Known GenesCWC27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer