A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417239



Internal ID21074792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28049896..28050300hg38UCSC Ensembl
chr8:27907413..27907817hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166137
Samples
Known GenesNUGGC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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