A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513773



Internal ID20887120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55879877..56003327hg38UCSC Ensembl
chr15:56172075..56295525hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38123451
hg19123451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024868
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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