A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739006



Internal ID20514978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88907374..88907433hg38UCSC Ensembl
chr6:89617093..89617152hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293876
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739006
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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