A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204473



Internal ID20771513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7888010..7913515hg38UCSC Ensembl
chr1:7948070..7973575hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3825506
hg1925506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334061
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204473
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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