A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419805



Internal ID21077358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108451308..108451674hg38UCSC Ensembl
chr8:109463537..109463903hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162205
Samples
Known GenesEMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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