A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516238



Internal ID20889599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43851578..43876086hg38UCSC Ensembl
chr19:44355730..44380238hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3824509
hg1924509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048127
Samples
Known GenesZNF404
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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