A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199212



Internal ID20766252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108016328..108034059hg38UCSC Ensembl
chr1:108558950..108576681hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817732
hg1917732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317584
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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