A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849634



Internal ID22624569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18143505..18165737hg38UCSC Ensembl
chr9:18143503..18165735hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3822233
hg1922233
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849634
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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