A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739616



Internal ID20515591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84701335..84701388hg38UCSC Ensembl
chr6:85411053..85411106hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739616
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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