A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381420



Internal ID22439290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36213677..36213989hg38UCSC Ensembl
chr18:33793640..33793952hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942205
Supporting Variants
Samples
Known GenesMOCOS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381420
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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