A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732172



Internal ID20508095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:909546..910093hg38UCSC Ensembl
chr6:909974..910443hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38548
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732172
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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