A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202056



Internal ID20769097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220484554..220490754hg38UCSC Ensembl
chr1:220657896..220664096hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg386201
hg196201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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