A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741398



Internal ID20517375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96035777..96035845hg38UCSC Ensembl
chr6:96483653..96483721hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283454
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741398
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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