A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743548



Internal ID20519536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132692641..132692705hg38UCSC Ensembl
chr6:133013780..133013844hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276279
Samples
Known GenesVNN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743548
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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