A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733207



Internal ID20509135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96712354..96712502hg38UCSC Ensembl
chr6:97160230..97160378hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733207
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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