A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007975



Internal ID20575015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109704782..109734274hg38UCSC Ensembl
chr13:110357129..110386621hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3829493
hg1929493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487881
Supporting Variants
Samples
Known GenesLINC00676
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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