A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499356



Internal ID20872575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65223718..65236081hg38UCSC Ensembl
chr15:65516056..65528419hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812364
hg1912364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499356
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