A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557260



Internal ID15997983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:6775910..6810403hg38UCSC Ensembl
Innerchr12:6885076..6919569hg19UCSC Ensembl
Innerchr12:6755337..6789830hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3834494
hg1934494
hg1834494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2323n54
Supporting Variantsnssv787256
Samples
Known GenesCD4, LAG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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