A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506723



Internal ID20880007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88233433..88247357hg38UCSC Ensembl
chr15:88776664..88790588hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3813925
hg1913925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180130
Samples
Known GenesNTRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506723
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