A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767452



Internal ID20543312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9328173..9328173hg38UCSC Ensembl
chr12:9480769..9480769hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767452
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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