A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15759111



Internal ID22093572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9129265..9129265hg38UCSC Ensembl
chr1:9189324..9189324hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15759111
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