A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028660



Internal ID21938003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124912606..124912832hg38UCSC Ensembl
chr12:125397152..125397378hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601549
Samples
Known GenesUBC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028660
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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