A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573366



Internal ID21521770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236038785..236038852hg38UCSC Ensembl
chr1:236202085..236202152hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063608
SamplesHG03009
Known GenesNID1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573366
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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