A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420353



Internal ID21077906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105028825..105169707hg38UCSC Ensembl
chr8:106041053..106181935hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38140883
hg19140883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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