A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925099



Internal ID21345168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30246697..30246774hg38UCSC Ensembl
chr8:30104213..30104290hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198738
SamplesHG002
Known GenesMIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925099
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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