A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940788



Internal ID21360857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99549037..99549037hg38UCSC Ensembl
chr7:99146660..99146660hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203122
SamplesHG002
Known GenesFAM200A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940788
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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