A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483492



Internal ID21141045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97448674..97449417hg38UCSC Ensembl
chr13:98100928..98101671hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015518
Samples
Known GenesRAP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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