A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496457



Internal ID20869659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3049580..3211239hg38UCSC Ensembl
chr17:2952874..3114533hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38161660
hg19161660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035381
Samples
Known GenesOR1A2, OR1D2, OR1D5, OR1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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