A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414432



Internal ID22472302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135657388..135861621hg38UCSC Ensembl
chr4:136578543..136782776hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38204234
hg19204234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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