A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730349



Internal ID20506260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110387237..110387302hg38UCSC Ensembl
chr12:110825042..110825107hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285482
Samples
Known GenesANAPC7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730349
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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