A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606725



Internal ID21555030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9080945..9080945hg38UCSC Ensembl
chr2:9221074..9221074hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115251
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606725
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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