A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199140



Internal ID20766180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187698654..187975363hg38UCSC Ensembl
chr1:187667786..187944494hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38276710
hg19276709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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