A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052527



Internal ID20619567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162842144..162846442hg38UCSC Ensembl
chr1:162811934..162816232hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052527
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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