A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009119



Internal ID20576161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44325595..44330127hg38UCSC Ensembl
chr13:44899731..44904263hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg384533
hg194533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490877
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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