A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092422



Internal ID20659463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101802363..101802922hg38UCSC Ensembl
chr3:101521207..101521766hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358133
Supporting Variants
Samples
Known GenesNXPE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00584


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