A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419668



Internal ID21077221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78895309..78896222hg38UCSC Ensembl
chr8:79807544..79808457hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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