A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099250



Internal ID20666290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30246947..30269197hg38UCSC Ensembl
chr3:30288438..30310688hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3822251
hg1922251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358141
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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