A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569786



Internal ID21518148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6304648..6306100hg38UCSC Ensembl
chr1:6364708..6366160hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381453
hg191453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066160
SamplesHG02011
Known GenesACOT7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569786
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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