A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584152



Internal ID21532688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82908752..82908870hg38UCSC Ensembl
chr5:82204571..82204689hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140586
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584152
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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