A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066523



Internal ID19155742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12451697..12491203hg38UCSC Ensembl
Innerchr19:12562511..12602017hg19UCSC Ensembl
Innerchr19:12423511..12463017hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839507
hg1939507
hg1839507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564763
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)nsv1066523
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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