A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579662



Internal ID16367071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42802004..43009115hg38UCSC Ensembl
Innerchr19:43306156..43513267hg19UCSC Ensembl
Innerchr19:47997996..48205107hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38207112
hg19207112
hg18207112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6465n54
Supporting Variantsnssv899645
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579662
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