A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744384



Internal ID20520383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8634161..8634280hg38UCSC Ensembl
chr18:8634159..8634278hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271629
Samples
Known GenesRAB12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744384
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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