A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530781



Internal ID20904142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36182139..36186131hg38UCSC Ensembl
chr19:36673041..36677033hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383993
hg193993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046334
Samples
Known GenesZNF565
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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