A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527119



Internal ID20900480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12188049..12188503hg38UCSC Ensembl
chr19:12298864..12299318hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044914
Samples
Known GenesZNF136
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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