A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368989



Internal ID22594658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232921323..232922062hg38UCSC Ensembl
chr1:233057069..233057808hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368989
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