A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381676



Internal ID22439546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25158189..25158850hg38UCSC Ensembl
chr18:22738153..22738814hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945138
Supporting Variants
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381676
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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