A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031016



Internal ID21940359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71285466..71285737hg38UCSC Ensembl
chr12:71679246..71679517hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031016
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer