A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571314



Internal ID21519691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146716295..146716621hg38UCSC Ensembl
chr6:147037431..147037757hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142722
SamplesNA19239
Known GenesADGB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571314
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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