A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423949



Internal ID21081502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30165301..30166100hg38UCSC Ensembl
chr8:30022817..30023616hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166837
Samples
Known GenesDCTN6, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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