A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579694



Internal ID16367103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42823854..43158934hg38UCSC Ensembl
Innerchr19:43328006..43663086hg19UCSC Ensembl
Innerchr19:48019846..48354926hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38335081
hg19335081
hg18335081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6467n54
Supporting Variantsnssv899703
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579694
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