A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023119



Internal ID21932462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32348723..32348777hg38UCSC Ensembl
chr12:32501657..32501711hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608813
Samples
Known GenesBICD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023119
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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