A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569772



Internal ID21518134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65613470..65613745hg38UCSC Ensembl
chr1:66079153..66079428hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066366
SamplesHG00512
Known GenesLEPR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569772
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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