A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372275



Internal ID22597944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3568920..3571760hg38UCSC Ensembl
chr18:3568918..3571758hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382841
hg192841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938575
Supporting Variants
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372275
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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