A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028031



Internal ID21937374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77888915..77891699hg38UCSC Ensembl
chr12:78282695..78285479hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg382785
hg192785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603276
Samples
Known GenesNAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028031
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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