A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465112



Internal ID22523001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92428625..92440258hg38UCSC Ensembl
chr13:93080878..93092511hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3811634
hg1911634
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863699
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465112
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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