A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294641



Internal ID20503859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147881455..147883645hg38UCSC Ensembl
chr4:148802606..148804796hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg382191
hg192191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749714
Supporting Variants
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294641
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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