A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426750



Internal ID21084303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29791953..29792406hg38UCSC Ensembl
chr8:29649469..29649922hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426750
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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