A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477212



Internal ID21134765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80341001..80341800hg38UCSC Ensembl
chr13:80915136..80915935hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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