A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519044



Internal ID20892405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76886356..76888256hg38UCSC Ensembl
chr18:74598312..74600212hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043899
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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