A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029525



Internal ID21938868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69807333..69807521hg38UCSC Ensembl
chr12:70201113..70201301hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603468
Samples
Known GenesRAB3IP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029525
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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