A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013606



Internal ID20580646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83907101..83913500hg38UCSC Ensembl
chr13:84481236..84487635hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00295


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