A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575952



Internal ID21524386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42804588..42805853hg38UCSC Ensembl
chr1:43270259..43271524hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065343
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575952
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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