A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028520



Internal ID21937863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19763012..19763903hg38UCSC Ensembl
chr12:19915946..19916837hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028520
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