A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576578



Internal ID21525018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185222021..185222235hg38UCSC Ensembl
chr4:186143175..186143389hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121846
SamplesHG03683
Known GenesSNX25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576578
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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