A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428093



Internal ID21085646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32117323..32117840hg38UCSC Ensembl
chr8:31974839..31975356hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168200
Samples
Known GenesNRG1, NRG1-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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