A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426719



Internal ID21084272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53041801..53081100hg38UCSC Ensembl
chr8:53954361..53993660hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3839300
hg1939300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7346n223
Supporting Variantsnssv18168350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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