A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493597



Internal ID22551526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166656956..166662626hg38UCSC Ensembl
chr4:167578107..167583777hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385671
hg195671
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838117
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493597
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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