A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983728



Internal ID21893071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27487548..27487614hg38UCSC Ensembl
chr1:27814059..27814125hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529573
Samples
Known GenesWASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983728
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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