A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893284



Internal ID15840554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7691330..7693453hg38UCSC Ensembl
Innerchr19:7756216..7758339hg19UCSC Ensembl
Innerchr19:7662216..7664339hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382124
hg192124
hg182124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578526
Supporting Variants
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893284
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