A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085694



Internal ID20652734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27247149..27252709hg38UCSC Ensembl
chr2:27470017..27475577hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg385561
hg195561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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