A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577943



Internal ID21526403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184231470..184231780hg38UCSC Ensembl
chr1:184200604..184200914hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061988
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577943
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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