A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935695



Internal ID22711040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21758610..21759371hg38UCSC Ensembl
chr18:19338571..19339332hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370918
Samples
Known GenesMIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935695
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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