A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371441



Internal ID22597110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83801661..83910464hg38UCSC Ensembl
chr16:83835266..83944069hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38108804
hg19108804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933986
Supporting Variants
Samples
Known GenesHSBP1, MLYCD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371441
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