A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485820



Internal ID21143373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46886916..46888656hg38UCSC Ensembl
chr13:47461051..47462791hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381741
hg191741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008553
Samples
Known GenesHTR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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