A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581473



Internal ID21529972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97433139..97438061hg38UCSC Ensembl
chr4:98354290..98359212hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg384923
hg194923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139405
SamplesNA24385
Known GenesSTPG2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581473
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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