A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416782



Internal ID21074335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33441156..33459924hg38UCSC Ensembl
chr8:33298674..33317442hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3818769
hg1918769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166632
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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