A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515940



Internal ID20889301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45385983..45386643hg38UCSC Ensembl
chr18:42965948..42966608hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041233
Samples
Known GenesSLC14A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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