A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415974



Internal ID21073527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65557280..65563641hg38UCSC Ensembl
chr8:66469515..66475876hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg386362
hg196362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169360
Samples
Known GenesLOC286186
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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