A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499151



Internal ID20872368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40497160..40504135hg38UCSC Ensembl
chr15:40789359..40796334hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386976
hg196976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499151
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