A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050759



Internal ID20617799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106585588..106587912hg38UCSC Ensembl
chr1:107128210..107130534hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg382325
hg192325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325969
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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