A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040440



Internal ID20607480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3740756..3741079hg38UCSC Ensembl
chr18:3740756..3741079hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528047
Supporting Variants
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00284


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