A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019657



Internal ID19108875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108293729..108341510hg38UCSC Ensembl
Innerchr5:107629430..107677211hg19UCSC Ensembl
Innerchr5:107657329..107705110hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3847782
hg1947782
hg1847782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5775n100
Supporting Variantsnssv3646996
Samples
Known GenesFBXL17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019657
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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