A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477644



Internal ID21135197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80839922..81005275hg38UCSC Ensembl
chr13:81414057..81579410hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38165354
hg19165354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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