A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733686



Internal ID20509616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133828319..133828464hg38UCSC Ensembl
chr9:136693441..136693586hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296474
Samples
Known GenesVAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733686
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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