A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565073



Internal ID21513383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76774377..76774452hg38UCSC Ensembl
chr1:77240062..77240137hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067271
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565073
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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