A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580143



Internal ID16020866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54054016..54056824hg38UCSC Ensembl
Innerchr19:54557270..54560078hg19UCSC Ensembl
Innerchr19:59249082..59251890hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382809
hg192809
hg182809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6546n54
Supporting Variantsnssv901368, nssv901371, nssv901374, nssv901376, nssv901377, nssv901367, nssv901378, nssv901369, nssv901375, nssv901372, nssv901373, nssv901370
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580143
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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