A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983902



Internal ID21893245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29214109..29214408hg38UCSC Ensembl
chr1:29540621..29540920hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535288
Samples
Known GenesMECR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983902
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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