A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423958



Internal ID21081511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13047871..13081440hg38UCSC Ensembl
chr8:12905380..12938949hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3833570
hg1933570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7261n223
Supporting Variantsnssv18165086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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