A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762199



Internal ID22096659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3356049..3356049hg38UCSC Ensembl
chr6:3356283..3356283hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4439323
Supporting Variants
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762199
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