A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911261



Internal ID22686474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107896000..107900423hg38UCSC Ensembl
chr9:110658281..110662704hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg384424
hg194424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911261
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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