A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096385



Internal ID20663425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154851319..154865466hg38UCSC Ensembl
chr3:154569108..154583255hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814148
hg1914148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370238
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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