A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110913



Internal ID20677953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153710348..153722272hg38UCSC Ensembl
chr4:154631500..154643424hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3811925
hg1911925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386013
Supporting Variants
Samples
Known GenesRNF175
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110913
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