A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731016



Internal ID20506934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170191584..170191850hg38UCSC Ensembl
chr6:170506808..170507074hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731016
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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