A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571201



Internal ID21519576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25441354..25441792hg38UCSC Ensembl
chr6:25441582..25442020hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154732
SamplesHG01114
Known GenesLRRC16A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571201
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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