A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205146



Internal ID20772186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82707310..82820737hg38UCSC Ensembl
chr1:83172993..83286420hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38113428
hg19113428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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