A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114502



Internal ID20681542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164543299..164814465hg38UCSC Ensembl
chr4:165464451..165735617hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38271167
hg19271167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391081
Supporting Variants
Samples
Known GenesLOC100505989, MIR5684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114502
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