A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458891



Internal ID22516772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37854855..37858054hg38UCSC Ensembl
chr13:38428992..38432191hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853178
Supporting Variants
Samples
Known GenesTRPC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458891
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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