A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571394



Internal ID21519772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158293113..158298901hg38UCSC Ensembl
chr4:159214265..159220053hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385789
hg195789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135442
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571394
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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