A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460058



Internal ID22517944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113925336..113936135hg38UCSC Ensembl
chr13:114628309..114639108hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856242
Supporting Variants
Samples
Known GenesLINC00565
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460058
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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