A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007125



Internal ID20574165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109933262..109933726hg38UCSC Ensembl
chr13:110585609..110586073hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481060
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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