A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518187



Internal ID20891548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28145901..28147700hg38UCSC Ensembl
chr18:25725865..25727664hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040716
Samples
Known GenesCDH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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