A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475158



Internal ID22533053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5807967..5815066hg38UCSC Ensembl
chr17:5711287..5718386hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872205
Supporting Variants
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475158
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