A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914535



Internal ID22689752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14999878..15000086hg38UCSC Ensembl
chr9:14999876..15000084hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437174
Samples
Known GenesLOC389705
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914535
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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