A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370425



Internal ID22596094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37851217..37858934hg38UCSC Ensembl
chr13:38425354..38433071hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg387718
hg197718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929080
Supporting Variants
Samples
Known GenesTRPC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370425
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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