A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456361



Internal ID22514239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50004558..50006969hg38UCSC Ensembl
chr13:50578694..50581105hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg382412
hg192412
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864169
Supporting Variants
Samples
Known GenesDLEU2, TRIM13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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