A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745729



Internal ID20521739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43011322..43012409hg38UCSC Ensembl
chr17:41163339..41164426hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265755
Samples
Known GenesIFI35
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745729
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