A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061308



Internal ID18803839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12471097..12581187hg38UCSC Ensembl
Innerchr19:12581911..12692001hg19UCSC Ensembl
Innerchr19:12442911..12553001hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38110091
hg19110091
hg18110091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3437n100
Supporting Variantsnssv3564771
Samples
Known GenesZNF490, ZNF564, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061308
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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