A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456752



Internal ID22514631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33669607..33677034hg38UCSC Ensembl
chr13:34243744..34251171hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg387428
hg197428
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853675
Supporting Variants
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456752
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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