A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483197



Internal ID21140750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46774779..46775446hg38UCSC Ensembl
chr13:47348914..47349581hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008543
Samples
Known GenesESD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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