A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv897578



Internal ID16191534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29566638..29567671hg38UCSC Ensembl
Innerchr19:30057545..30058578hg19UCSC Ensembl
Innerchr19:34749385..34750418hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381034
hg191034
hg181034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579276
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv897578
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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