A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030351



Internal ID21939694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12175282..12175580hg38UCSC Ensembl
chr12:12328216..12328514hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601577
Samples
Known GenesLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030351
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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