A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737576



Internal ID20513538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55443010..55443077hg38UCSC Ensembl
chr6:55307808..55307875hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267479
Samples
Known GenesHMGCLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737576
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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