A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863699



Internal ID22638634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92428625..92440258hg38UCSC Ensembl
chr13:93080878..93092511hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3811634
hg1911634
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465112
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863699
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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