A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762534



Internal ID20538394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44805347..44805347hg38UCSC Ensembl
chr4:44807364..44807364hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762534
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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