A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026382



Internal ID21935725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9606705..9606760hg38UCSC Ensembl
chr12:9759301..9759356hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606011
Samples
Known GenesKLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026382
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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