A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415854



Internal ID21073407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66698552..66709384hg38UCSC Ensembl
chr8:67610787..67621619hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3810833
hg1910833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169423
Samples
Known GenesC8orf44-SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415854
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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