A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063446



Internal ID19152665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12408389..12431081hg38UCSC Ensembl
Innerchr19:12519203..12541895hg19UCSC Ensembl
Innerchr19:12380203..12402895hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3822693
hg1922693
hg1822693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3433n100
Supporting Variantsnssv3564752, nssv3564753
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063446
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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