A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733616



Internal ID20509546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56261790..56263761hg38UCSC Ensembl
chr18:53929021..53930992hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg381972
hg191972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733616
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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