A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420955



Internal ID21078508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104268870..104269855hg38UCSC Ensembl
chr8:105281098..105282083hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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