A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617490



Internal ID21565795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25902094..25902094hg38UCSC Ensembl
chr1:26228585..26228585hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064292
SamplesNA19238
Known GenesSTMN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617490
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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