A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012194



Internal ID21921537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124898380..124898434hg38UCSC Ensembl
chr5:124234073..124234127hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012194
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