A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027540



Internal ID21936883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13899389..13899879hg38UCSC Ensembl
chr12:14052323..14052813hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615648
Samples
Known GenesGRIN2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027540
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