A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475155



Internal ID22533050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57938505..57942521hg38UCSC Ensembl
chr17:56015866..56019882hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384017
hg194017
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874621
Supporting Variants
Samples
Known GenesCUEDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475155
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