A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607871



Internal ID21556176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90891782..90891782hg38UCSC Ensembl
chr1:91357339..91357339hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067093
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607871
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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