A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459598



Internal ID22517484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59989686..60055150hg38UCSC Ensembl
chr13:60563820..60629284hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3865465
hg1965465
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862307
Supporting Variants
Samples
Known GenesDIAPH3, DIAPH3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459598
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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