A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611398



Internal ID16398807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:56141307..56184579hg38UCSC Ensembl
Innerchr8:57053866..57097138hg19UCSC Ensembl
Innerchr8:57216420..57259692hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3843273
hg1943273
hg1843273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12174n54
Supporting Variantsnssv1115583, nssv1115582
Samples
Known GenesPLAG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611398
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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