A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199201



Internal ID20766241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106560478..106594165hg38UCSC Ensembl
chr1:107103100..107136787hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3833688
hg1933688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318979
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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