A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515886



Internal ID20889247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37417937..37437530hg38UCSC Ensembl
chr18:34997900..35017493hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3819594
hg1919594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040441
Samples
Known GenesCELF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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