A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375442



Internal ID22601111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26053317..26053665hg38UCSC Ensembl
chr18:23633281..23633629hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932192
Supporting Variants
Samples
Known GenesSS18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375442
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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