A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435488



Internal ID21397490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30746374..30747881hg38UCSC Ensembl
chr8:30603891..30605398hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381508
hg191508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n172
Supporting Variantsnssv15749630
SamplesNB07
Known GenesUBXN8
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435488
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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