A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565769



Internal ID21757734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32267060..32267189hg38UCSC Ensembl
chr8:32124576..32124705hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012323
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565769
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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