A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512571



Internal ID20885906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62342437..62345549hg38UCSC Ensembl
chr15:62634636..62637748hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383113
hg193113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025588
Samples
Known GenesMIR6085
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512571
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