A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588456



Internal ID16029179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22416581..22881878hg38UCSC Ensembl
Innerchr22:22770917..23224058hg19UCSC Ensembl
Innerchr22:21100917..21554058hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38465298
hg19453142
hg18453142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8005n54
Supporting Variantsnssv1152108, nssv1152109
Samples1798860443_A, 1798860280_A
Known GenesGGTLC2, LOC648691, MIR650, POM121L1P, PRAME, ZNF280A, ZNF280B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588456
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