A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625889



Internal ID21574194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80432000..80432000hg38UCSC Ensembl
chr6:81141717..81141717hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140706
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625889
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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