A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920786



Internal ID22696009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74086765..74089717hg38UCSC Ensembl
chr9:76701681..76704633hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382953
hg192953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432462
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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