A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847679



Internal ID22622614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42833393..42843235hg38UCSC Ensembl
chr9:44127884..44137726hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389843
hg199843
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2117n209
Supporting Variantsnssv17513489, nssv17513488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847679
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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