A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764908



Internal ID20540768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167434894..167434894hg38UCSC Ensembl
chr1:167404131..167404131hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277405
Samples
Known GenesCD247
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764908
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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