A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495768



Internal ID20868962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45025901..45032100hg38UCSC Ensembl
chr15:45318099..45324298hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184280
Samples
Known GenesSORD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495768
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