A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566472



Internal ID21514798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8026903..8027208hg38UCSC Ensembl
chr5:8027016..8027321hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143751
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566472
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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