A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107432



Internal ID20674472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100823549..100826941hg38UCSC Ensembl
chr4:101744706..101748098hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg383393
hg193393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107432
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