A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028329



Internal ID21937672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110387304..110387370hg38UCSC Ensembl
chr12:110825109..110825175hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610993
Samples
Known GenesANAPC7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028329
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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