A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936890



Internal ID22712251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110383797..110384124hg38UCSC Ensembl
chr12:110821602..110821929hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368507
Samples
Known GenesANAPC7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936890
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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