A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433913



Internal ID21395915
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 StatusM
Merged Variantsdgv533n172
Supporting Variantsnssv15751333, nssv15753307, nssv15745856
SamplesSMI041, SMI018, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433913
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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