A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051873



Internal ID20618913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117534508..117539697hg38UCSC Ensembl
chr1:118077130..118082319hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg385190
hg195190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051873
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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