A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066747



Internal ID18809278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20803118hg38UCSC Ensembl
Innerchr19:20829579..20985924hg19UCSC Ensembl
Innerchr19:20621419..20777764hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38156346
hg19156346
hg18156346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3570558
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066747
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