A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933782



Internal ID21353851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99588977..99588977hg38UCSC Ensembl
chr4:100510134..100510134hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201186
SamplesHG002
Known GenesMTTP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933782
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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