A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559784



Internal ID16000507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:93570897..93572036hg38UCSC Ensembl
Innerchr12:93964673..93965812hg19UCSC Ensembl
Innerchr12:92488804..92489943hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381140
hg191140
hg181140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n54
Supporting Variantsnssv800713
Samples
Known GenesSOCS2, SOCS2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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