A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570211



Internal ID21518575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102463827..102464078hg38UCSC Ensembl
chr4:103384984..103385235hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121053
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570211
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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