A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922733



Internal ID22697958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124945294..124945427hg38UCSC Ensembl
chr9:127707573..127707706hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441128
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922733
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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