A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572421



Internal ID21520811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60418287..60418348hg38UCSC Ensembl
chr2:60645422..60645483hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114579
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572421
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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