A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462008



Internal ID22519893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98535532..98536531hg38UCSC Ensembl
chr13:99187786..99188785hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852088
Supporting Variants
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462008
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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