A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742946



Internal ID20518932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147798745..147798799hg38UCSC Ensembl
chr4:148719896..148719950hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266618
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742946
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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