A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735181



Internal ID20511122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45560846..45562628hg38UCSC Ensembl
chr1:46026518..46028300hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381783
hg191783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272535
Samples
Known GenesAKR1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735181
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