A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044929



Internal ID20611969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12388560..12428062hg38UCSC Ensembl
chr19:12499374..12538876hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839503
hg1939503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519849
Supporting Variants
Samples
Known GenesZNF799
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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