A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910780



Internal ID22685991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127834788..127835250hg38UCSC Ensembl
chr9:130597067..130597529hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447126
Samples
Known GenesENG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910780
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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