A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583711



Internal ID21532239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28901201..28901361hg38UCSC Ensembl
chr1:29227713..29227873hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064948
SamplesHG00732
Known GenesEPB41
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583711
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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