A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912645



Internal ID22687861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43103818..43110040hg38UCSC Ensembl
chr9:42875237..42881409hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386223
hg196173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432756
Samples
Known GenesAQP7P3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912645
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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