A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754615



Internal ID20530475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97132608..97132608hg38UCSC Ensembl
chr12:97526386..97526386hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754615
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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