A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854656



Internal ID22629591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29716607..29717606hg38UCSC Ensembl
chr9:29716605..29717604hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854656
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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