A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444456



Internal ID22110636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36810862..36810862hg38UCSC Ensembl
chr14:37280067..37280067hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765116
Samples
Known GenesSLC25A21
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444456
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