A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029214



Internal ID21938557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:126244988..126254623hg38UCSC Ensembl
chr12:126729534..126739169hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg389636
hg199636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029214
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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