A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487417



Internal ID21144970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70683103..70695815hg38UCSC Ensembl
chr13:71257235..71269947hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3812713
hg1912713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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