A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050746



Internal ID20617786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106482897..106483601hg38UCSC Ensembl
chr1:107025519..107026223hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050746
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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