A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493364



Internal ID22551293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23643177..23652763hg38UCSC Ensembl
chr4:23644800..23654386hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg389587
hg199587
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493364
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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