A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194606



Internal ID21333471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75123269..75123269hg38UCSC Ensembl
chr15:75415610..75415610hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935057
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194606
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