A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499806



Internal ID22557742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44663698..44666397hg38UCSC Ensembl
chr5:44663800..44666499hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499806
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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