A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056879



Internal ID18799410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20643872..20790626hg38UCSC Ensembl
Innerchr19:20826678..20973432hg19UCSC Ensembl
Innerchr19:20618518..20765272hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38146755
hg19146755
hg18146755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3570544
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)nsv1056879
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