A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610993



Internal ID21803040
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 StatusS
Merged Variantsnsv6028329
Supporting Variants
Samples
Known GenesANAPC7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610993
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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