A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853722



Internal ID22628657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17098031..17113530hg38UCSC Ensembl
chr9:17098029..17113528hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3815500
hg1915500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853722
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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