A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428652



Internal ID21086205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15503284..15504160hg38UCSC Ensembl
chr8:15360793..15361669hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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