A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152066



Internal ID20719106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105582719..105589210hg38UCSC Ensembl
chr7:105223166..105229657hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg386492
hg196492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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