A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578625



Internal ID16366034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12398722..12437680hg38UCSC Ensembl
Innerchr19:12509536..12548494hg19UCSC Ensembl
Innerchr19:12370536..12409494hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3838959
hg1938959
hg1838959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893563
Samples
Known GenesZNF443, ZNF799
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578625
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