A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745856



Internal ID21391471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154821250..154836113hg38UCSC Ensembl
chr3:154539039..154553902hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814864
hg1914864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433913
Supporting Variants
SamplesSMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745856
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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