A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582864



Internal ID21531381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54905716..54906495hg38UCSC Ensembl
chr1:55371389..55372168hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065456
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582864
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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