A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739731



Internal ID20515706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96132258..96132360hg38UCSC Ensembl
chr6:96580134..96580236hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291339
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739731
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer