A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477041



Internal ID21134594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82470336..82471064hg38UCSC Ensembl
chr13:83044471..83045199hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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