A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075531



Internal ID20642571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102044847..102057259hg38UCSC Ensembl
chr2:102661309..102673720hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3812413
hg1912412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6338163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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