A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571309



Internal ID21519686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53675607..53677596hg38UCSC Ensembl
chr4:54541774..54543763hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125469
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571309
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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