A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099157



Internal ID20666197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40669485..40673386hg38UCSC Ensembl
chr3:40710976..40714877hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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