A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078900



Internal ID21988133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32651286..32651286hg38UCSC Ensembl
chr8:32508805..32508805hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573515
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078900
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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