A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416188



Internal ID21073741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53493406..53493698hg38UCSC Ensembl
chr8:54405966..54406258hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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