A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136660



Internal ID20703700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110074849..110093032hg38UCSC Ensembl
chr6:110396052..110414235hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3818184
hg1918184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613886
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01254


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