A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852527



Internal ID22627462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39471913..39478755hg38UCSC Ensembl
chr9:41616931..41623773hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386843
hg196843
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2104n209
Supporting Variantsnssv17513116, nssv17513115, nssv17513114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852527
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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