A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190686



Internal ID21329546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3085812..3085812hg38UCSC Ensembl
chr10:3128004..3128004hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937656
Supporting Variants
SamplesHG002
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190686
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