A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578561



Internal ID16019284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8504851..8564616hg38UCSC Ensembl
Innerchr19:8569735..8629500hg19UCSC Ensembl
Innerchr19:8475735..8535500hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3859766
hg1959766
hg1859766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6258n54
Supporting Variantsnssv1150040, nssv1150039
Samples1780862300_A, 1780862306_A
Known GenesMYO1F, ZNF414
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578561
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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