A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578811



Internal ID16019534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20379052..20584511hg38UCSC Ensembl
Innerchr19:20489861..20767317hg19UCSC Ensembl
Innerchr19:20350861..20559157hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38205460
hg19277457
hg18208297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6304n54
Supporting Variantsnssv896166
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF737, ZNF826P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578811
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