A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606217



Internal ID21554522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211609083..211609083hg38UCSC Ensembl
chr1:211782425..211782425hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062278
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606217
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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