A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497564



Internal ID20870771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50148513..50158529hg38UCSC Ensembl
chr15:50440710..50450726hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3810017
hg1910017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497564
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