A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052063



Internal ID20619103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15515849..15516321hg38UCSC Ensembl
chr1:15842344..15842816hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318028
Supporting Variants
Samples
Known GenesCASP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00164


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