A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457938



Internal ID22515819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92079303..92098423hg38UCSC Ensembl
chr13:92731556..92750676hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3819121
hg1919121
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859084
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457938
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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