A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476680



Internal ID21134233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109824305..109847687hg38UCSC Ensembl
chr13:110476652..110500034hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3823383
hg1923383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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