A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372072



Internal ID22597741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85657971..85677234hg38UCSC Ensembl
chr1:86123654..86142917hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3819264
hg1919264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880346
Supporting Variants
Samples
Known GenesZNHIT6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372072
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