A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517024



Internal ID20890385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69484084..69484638hg38UCSC Ensembl
chr17:67480225..67480779hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037642
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517024
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