A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051343



Internal ID20618383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151604112..151609174hg38UCSC Ensembl
chr1:151576588..151581650hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg385063
hg195063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334727
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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