A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765781



Internal ID22100261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92120376..92120376hg38UCSC Ensembl
chr14:92586720..92586720hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445645
Supporting Variants
Samples
Known GenesNDUFB1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765781
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer