A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494365



Internal ID22552295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22449275..22452938hg38UCSC Ensembl
chr4:22450898..22454561hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383664
hg193664
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839513
Supporting Variants
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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