A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513896



Internal ID20887245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96329501..96335300hg38UCSC Ensembl
chr15:96872730..96878529hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2634n223
Supporting Variantsnssv18188192
Samples
Known GenesMIR1469, NR2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer