A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204332



Internal ID20771372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69567001..69569100hg38UCSC Ensembl
chr1:70032684..70034783hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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