A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856425



Internal ID22631360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27863337..27871599hg38UCSC Ensembl
chr9:27863335..27871597hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg388263
hg198263
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856425
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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