A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951170



Internal ID21371239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34506225..34506225hg38UCSC Ensembl
chr13:35080362..35080362hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194097, nssv15194098
SamplesHG002
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951170
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