A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493587



Internal ID22551516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164694979..164729410hg38UCSC Ensembl
chr4:165616131..165650562hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3834432
hg1934432
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837804
Supporting Variants
Samples
Known GenesMIR5684
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493587
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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