A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853433



Internal ID22628368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17567653..17577653hg38UCSC Ensembl
chr10:17609652..17619652hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853433
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