A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099296



Internal ID20666336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30695201..30758500hg38UCSC Ensembl
chr3:30736693..30799992hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3863300
hg1963300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360411
Supporting Variants
Samples
Known GenesGADL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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