A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573470



Internal ID21521876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89607815..89607938hg38UCSC Ensembl
chr6:90317534..90317657hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153363
SamplesNA19239
Known GenesANKRD6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573470
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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