A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv897034



Internal ID16190990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27242739..27471004hg38UCSC Ensembl
Innerchr19:27733647..27961912hg19UCSC Ensembl
Innerchr19:32425487..32653752hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38228266
hg19228266
hg18228266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579124
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)nssv897034
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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