A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429886



Internal ID21087439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109157089..109294588hg38UCSC Ensembl
chr8:110169318..110306817hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38137500
hg19137500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162846
Samples
Known GenesNUDCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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