A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476653



Internal ID21134206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26967555..26971830hg38UCSC Ensembl
chr13:27541692..27545967hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg384276
hg194276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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