A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853863



Internal ID22628798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92090099..92113471hg38UCSC Ensembl
chr13:92742352..92765724hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3823373
hg1923373
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468984
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853863
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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