A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580407



Internal ID21528897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143875316..143878740hg38UCSC Ensembl
chr6:144196453..144199877hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383425
hg193425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150256
SamplesHG00732
Known GenesZC2HC1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580407
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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