A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502270



Internal ID20875513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58508399..58575210hg38UCSC Ensembl
chr15:58800598..58867409hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3866812
hg1966812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026174
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502270
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