A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625152



Internal ID21573457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163291263..163291263hg38UCSC Ensembl
chr6:163712295..163712295hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155766
SamplesNA19238
Known GenesPACRG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625152
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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