A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557403



Internal ID16344812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9464487..9573873hg38UCSC Ensembl
Innerchr12:9617083..9726469hg19UCSC Ensembl
Innerchr12:9508350..9617736hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38109387
hg19109387
hg18109387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2349n54
Supporting Variantsnssv787553
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557403
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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