A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047648



Internal ID20614688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32382472..32383297hg38UCSC Ensembl
chr19:32873378..32874203hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519209
Supporting Variants
Samples
Known GenesZNF507
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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