A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497243



Internal ID22555177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76112181..76132787hg38UCSC Ensembl
chr4:77033334..77053940hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3820607
hg1920607
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839798
Supporting Variants
Samples
Known GenesART3, NUP54
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497243
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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