A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385703



Internal ID22443573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98511455..98604325hg38UCSC Ensembl
chr13:99163709..99256579hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3892871
hg1992871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942411
Supporting Variants
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385703
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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