A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578091



Internal ID16018814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:411849..431187hg38UCSC Ensembl
Innerchr19:411849..431187hg19UCSC Ensembl
Innerchr19:362849..382187hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3819339
hg1919339
hg1819339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv890996
Samples
Known GenesSHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578091
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