A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767445



Internal ID20543305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181124474..181124474hg38UCSC Ensembl
chr1:181093610..181093610hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767445
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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