A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876730



Internal ID22651691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36407997..36418888hg38UCSC Ensembl
chr18:33987960..33998851hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3810892
hg1910892
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477918
Samples
Known GenesFHOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876730
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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