A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761676



Internal ID20537536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30362469..30362469hg38UCSC Ensembl
chr12:30515402..30515402hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277976
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761676
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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