A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035333



Internal ID21944676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11247604..11390043hg38UCSC Ensembl
chr12:11400511..11542977hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38142440
hg19142467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613573
Samples
Known GenesPRB1, PRB3, PRB4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035333
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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