A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984984



Internal ID21894327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9123488..9123552hg38UCSC Ensembl
chr1:9183547..9183611hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530065
Samples
Known GenesGPR157
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984984
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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