A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578337



Internal ID16019060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1808864..1904613hg38UCSC Ensembl
Innerchr19:1808863..1904612hg19UCSC Ensembl
Innerchr19:1759863..1855612hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3895750
hg1995750
hg1895750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891943
Samples
Known GenesABHD17A, ATP8B3, KLF16, LOC100288123, MIR1909, REXO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578337
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