A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732947



Internal ID20508873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167940195..167940996hg38UCSC Ensembl
chr6:168340875..168341676hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273715
Samples
Known GenesMLLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732947
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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