A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010860



Internal ID20577900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61532832..61536687hg38UCSC Ensembl
chr13:62106965..62110820hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg383856
hg193856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480337
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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