A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475936



Internal ID21133489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89278066..89278740hg38UCSC Ensembl
chr13:89930320..89930994hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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