A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059473



Internal ID18802004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28373028..29130526hg38UCSC Ensembl
Innerchr19:28863935..29621433hg19UCSC Ensembl
Innerchr19:33555775..34313273hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38757499
hg19757499
hg18757499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724351
Samples
Known GenesLINC00906, LOC100505835
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059473
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