A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428930



Internal ID21086483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84800747..84834731hg38UCSC Ensembl
chr8:85712982..85746966hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3833985
hg1933985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172004
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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