A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575859



Internal ID21524291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180869406..180869686hg38UCSC Ensembl
chr1:180838542..180838822hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061445
SamplesNA20509
Known GenesXPR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575859
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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