A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511906



Internal ID288474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53101167..53102226hg38UCSC Ensembl
chr12:53494951..53496010hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17058628
Samples
Known GenesIGFBP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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