A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934261



Internal ID21354330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101849672..101849672hg38UCSC Ensembl
chr14:102316009..102316009hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193713
SamplesHG002
Known GenesPPP2R5C
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934261
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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