A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847887



Internal ID22622822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27274021..27295398hg38UCSC Ensembl
chr9:27274019..27295396hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3821378
hg1921378
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2091n209
Supporting Variantsnssv17512572
Samples
Known GenesEQTN, LINC00032
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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