A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074671



Internal ID20641711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100535534..100538389hg38UCSC Ensembl
chr2:101151996..101154851hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382856
hg192856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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