A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382687



Internal ID22440557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62327842..62327944hg38UCSC Ensembl
chr13:62901975..62902077hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382687
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