A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477918



Internal ID22535819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36407997..36418888hg38UCSC Ensembl
chr18:33987960..33998851hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3810892
hg1910892
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876730
Supporting Variants
Samples
Known GenesFHOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477918
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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