A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472016



Internal ID22529908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68846262..68875357hg38UCSC Ensembl
chr18:66513499..66542594hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3829096
hg1929096
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880845
Supporting Variants
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472016
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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