A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572368



Internal ID21520757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79432059..79432523hg38UCSC Ensembl
chr1:79897744..79898208hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066135
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572368
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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