A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074669



Internal ID20641709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100508136..100510866hg38UCSC Ensembl
chr2:101124598..101127328hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382731
hg192731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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