A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040004



Internal ID20607044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32954228..32954638hg38UCSC Ensembl
chr18:30534192..30534602hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529943
Supporting Variants
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00112


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