A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528353



Internal ID20901714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37488943..37489361hg38UCSC Ensembl
chr18:35068906..35069324hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040443
Samples
Known GenesCELF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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