A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177653



Internal ID20744693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36373008..36375792hg38UCSC Ensembl
chr18:33952971..33955755hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382785
hg192785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527318
Supporting Variants
Samples
Known GenesFHOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00038


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