A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5393n54



Internal ID22773288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:820999..821358hg38UCSC Ensembl
chr17:724239..724598hg19UCSC Ensembl
chr17:670989..671348hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38360
hg19360
hg18360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574094, nsv574093
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5393n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss728
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer