A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498234



Internal ID22556169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114810170..114813666hg38UCSC Ensembl
chr4:115731326..115734822hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498234
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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