A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496019



Internal ID22553952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59154174..59157864hg38UCSC Ensembl
chr4:60019892..60023582hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg383691
hg193691
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496019
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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