A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570905



Internal ID21519276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6185335..6185422hg38UCSC Ensembl
chr6:6185568..6185655hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158351
SamplesHG03683
Known GenesF13A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570905
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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