A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373994



Internal ID22599663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113617547..113617610hg38UCSC Ensembl
chr13:114271862..114271925hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940222
Supporting Variants
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373994
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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