A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424181



Internal ID21081734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96852980..96859237hg38UCSC Ensembl
chr8:97865208..97871465hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg386258
hg196258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173817
Samples
Known GenesCPQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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