A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891138



Internal ID16185094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:517392..518897hg38UCSC Ensembl
Innerchr19:517392..518897hg19UCSC Ensembl
Innerchr19:468392..469897hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381506
hg191506
hg181506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578125
Supporting Variants
Samples
Known GenesTPGS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891138
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