A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886575



Internal ID22661564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53678415..53718221hg38UCSC Ensembl
chr17:51755776..51795582hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3839807
hg1939807
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886575
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