A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925780



Internal ID22701007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85383162..85383250hg38UCSC Ensembl
chr9:87998077..87998165hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925780
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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