A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530457



Internal ID20903818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20175686..22871251hg38UCSC Ensembl
chr19:20286495..23054053hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg382695566
hg192767559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198404
Samples
Known GenesLINC00664, LOC100996349, LOC440518, LOC641367, MIR1270-1, MIR1270-2, ZNF100, ZNF208, ZNF257, ZNF429, ZNF43, ZNF430, ZNF431, ZNF486, ZNF492, ZNF493, ZNF626, ZNF676, ZNF708, ZNF714, ZNF729, ZNF737, ZNF738, ZNF826P, ZNF85, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530457
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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