A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041686



Internal ID20608726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3523132..3523657hg38UCSC Ensembl
chr18:3523130..3523655hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526830
Supporting Variants
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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