A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531986



Internal ID20905347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44291798..44336656hg38UCSC Ensembl
chr19:44795951..44840809hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3844859
hg1944859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198840
Samples
Known GenesZNF112, ZNF235
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531986
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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