A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059260



Internal ID19148479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12466648..12499043hg38UCSC Ensembl
Innerchr19:12577462..12609857hg19UCSC Ensembl
Innerchr19:12438462..12470857hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3832396
hg1932396
hg1832396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564770
Samples
Known GenesZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059260
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