A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948677



Internal ID21368746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151678620..151678620hg38UCSC Ensembl
chr4:152599772..152599772hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201243
SamplesHG002
Known GenesPET112
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948677
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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