A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877009



Internal ID22651972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19427970..19429369hg38UCSC Ensembl
chr17:19331283..19332682hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877009
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