A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524005



Internal ID21848364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150226797..150229072hg38UCSC Ensembl
chr1:150199129..150201405hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg382276
hg192277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981131
Supporting Variants
Samples
Known GenesANP32E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524005
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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