A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582861



Internal ID21531378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155596943..155597001hg38UCSC Ensembl
chr5:154976503..154976561hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122104
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582861
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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