A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499656



Internal ID20872878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35558901..35561300hg38UCSC Ensembl
chr15:35851102..35853501hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023416
Samples
Known GenesDPH6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499656
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