A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044863



Internal ID20611903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11615101..11616500hg38UCSC Ensembl
chr19:11725916..11727315hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525050
Supporting Variants
Samples
Known GenesZNF627
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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