A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767252



Internal ID20543112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23731270..23731270hg38UCSC Ensembl
chr6:23731498..23731498hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767252
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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