A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040813



Internal ID20607853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33440136..33446007hg38UCSC Ensembl
chr18:31020100..31025971hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg385872
hg195872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525815
Supporting Variants
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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