A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567514



Internal ID21515852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61907877..61908030hg38UCSC Ensembl
chr5:61203704..61203857hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145361
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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