A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531498



Internal ID20904859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69484464..69494759hg38UCSC Ensembl
chr17:67480605..67490900hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3810296
hg1910296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n223
Supporting Variantsnssv18037643
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531498
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