A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851746



Internal ID22626681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42925176..42940042hg38UCSC Ensembl
chr9:44031077..44045943hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3814867
hg1914867
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513514, nssv17513513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851746
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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