A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119202



Internal ID20686242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62774818..62775369hg38UCSC Ensembl
chr4:63640536..63641087hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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