A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921315



Internal ID22696538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111957117..111957629hg38UCSC Ensembl
chr9:114719397..114719909hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921315
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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