A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534744



Internal ID20908105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21782475..21783888hg38UCSC Ensembl
chr18:19362436..19363849hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381414
hg191414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040260
Samples
Known GenesMIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534744
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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