A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530926



Internal ID20904287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65118530..65122465hg38UCSC Ensembl
chr17:63114648..63118583hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg383936
hg193936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530926
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