A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574991



Internal ID21523414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171439776..171442857hg38UCSC Ensembl
chr1:171408915..171411996hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg383082
hg193082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061338
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574991
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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