A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879222



Internal ID22654191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9778057..9786183hg38UCSC Ensembl
chr17:9681374..9689500hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg388127
hg198127
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479530
Samples
Known GenesDHRS7C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879222
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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