A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080422



Internal ID20647463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172361051..172362454hg38UCSC Ensembl
chr2:173225779..173227182hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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