A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128439



Internal ID20695479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163656146..163659871hg38UCSC Ensembl
chr5:163083152..163086877hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg383726
hg193726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400003
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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