A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730418



Internal ID20506330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94934479..94934548hg38UCSC Ensembl
chr8:95946707..95946776hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296144
Samples
Known GenesTP53INP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730418
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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