A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926316



Internal ID22701543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13250916..13252635hg38UCSC Ensembl
chr9:13250915..13252634hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381720
hg191720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444675
Samples
Known GenesMPDZ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926316
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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