A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057477



Internal ID20624517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218442101..218442800hg38UCSC Ensembl
chr1:218615443..218616142hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316656
Supporting Variants
Samples
Known GenesTGFB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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