A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610941



Internal ID21559246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56413381..56413381hg38UCSC Ensembl
chr1:56879053..56879053hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065642
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610941
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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