A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435489



Internal ID21397491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30746541..30748023hg38UCSC Ensembl
chr8:30604058..30605540hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381483
hg191483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n172
Supporting Variantsnssv15753242
SamplesNB10
Known GenesUBXN8
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435489
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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