A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421921



Internal ID21079474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70290201..70292400hg38UCSC Ensembl
chr8:71202436..71204635hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169550
Samples
Known GenesNCOA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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