A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431930



Internal ID21089483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35085361..35086076hg38UCSC Ensembl
chr8:34942879..34943594hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38716
hg19716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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