A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064808



Internal ID20631848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85454682..85457156hg38UCSC Ensembl
chr1:85920365..85922839hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334069
Supporting Variants
Samples
Known GenesDDAH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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