A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387994



Internal ID22445864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53051264..53051341hg38UCSC Ensembl
chr13:53625399..53625476hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941344
Supporting Variants
Samples
Known GenesOLFM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387994
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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