A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218081



Internal ID20785121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11066001..11079500hg38UCSC Ensembl
chr8:10923511..10937010hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3813500
hg1913500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425508
Supporting Variants
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218081
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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