A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029055



Internal ID21938398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6557920..6557982hg38UCSC Ensembl
chr12:6667086..6667148hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616869
Samples
Known GenesNOP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029055
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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