A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580380



Internal ID21528870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101036724..101039019hg38UCSC Ensembl
chr6:101484600..101486895hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382296
hg192296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148011
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580380
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