A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025222



Internal ID21934565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102097383..102097507hg38UCSC Ensembl
chr12:102491161..102491285hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606804
Samples
Known GenesNUP37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025222
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