A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518300



Internal ID20891661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21501445..23112121hg38UCSC Ensembl
chr19:21684247..23294923hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381610677
hg191610677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3477n223
Supporting Variantsnssv18198470
Samples
Known GenesLINC00664, LOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF429, ZNF43, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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