A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531380



Internal ID20904741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33393395..33406948hg38UCSC Ensembl
chr18:30973359..30986912hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3813554
hg1913554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040807
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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