A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010462



Internal ID20577502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59122201..59123000hg38UCSC Ensembl
chr13:59696335..59697134hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494169
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00118


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