A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059683



Internal ID18802214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358579..35379534hg38UCSC Ensembl
Innerchr19:35849481..35870436hg19UCSC Ensembl
Innerchr19:40541321..40562276hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3820956
hg1920956
hg1820956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3521n100
Supporting Variantsnssv3568146
Samples
Known GenesFFAR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059683
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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