A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847627



Internal ID22622562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133179427..133187200hg38UCSC Ensembl
chr9:136054814..136062587hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387774
hg197774
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847627
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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