A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767231



Internal ID20543091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2781614..2781614hg38UCSC Ensembl
chr9:2781614..2781614hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767231
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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