A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575484



Internal ID21523913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206151230..206151373hg38UCSC Ensembl
chr1:206189957..206190100hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062749
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575484
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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