A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579358



Internal ID21527837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63239685..63242474hg38UCSC Ensembl
chr1:63705356..63708145hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382790
hg192790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066168
SamplesHG00512
Known GenesLINC00466
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579358
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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