A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932433



Internal ID22707731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3600291..3601341hg38UCSC Ensembl
chr18:3600289..3601339hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385959
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932433
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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