A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574412



Internal ID21766455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32267325..32267325hg38UCSC Ensembl
chr8:32124841..32124841hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063383
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574412
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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