A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045239



Internal ID20612279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2269101..2269600hg38UCSC Ensembl
chr19:2269100..2269599hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531232
Supporting Variants
Samples
Known GenesOAZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0017


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