A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429929



Internal ID21087482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31892741..31893140hg38UCSC Ensembl
chr8:31750257..31750656hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168183
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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