A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534990



Internal ID20908351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32902814..32961164hg38UCSC Ensembl
chr18:30482778..30541128hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3858351
hg1958351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039999
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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