A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737079



Internal ID20513036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159507592..159507651hg38UCSC Ensembl
chr6:159928624..159928683hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737079
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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