A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611691



Internal ID21559996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2019220..2019220hg38UCSC Ensembl
chr1:1950659..1950659hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062423
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611691
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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