A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484582



Internal ID21142135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46158801..46166300hg38UCSC Ensembl
chr13:46732936..46740435hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177793
Samples
Known GenesLCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484582
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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