A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500471



Internal ID20873698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62331284..62384378hg38UCSC Ensembl
chr15:62623483..62676577hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3853095
hg1953095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025586
Samples
Known GenesMIR6085
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500471
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