A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570818



Internal ID21519188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4566298..4566895hg38UCSC Ensembl
chr4:4568025..4568622hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132687
SamplesHG03125
Known GenesSTX18-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570818
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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