A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557888



Internal ID16345297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29005250..29010358hg38UCSC Ensembl
Innerchr12:29158183..29163291hg19UCSC Ensembl
Innerchr12:29049450..29054558hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg385109
hg195109
hg185109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2438n54
Supporting Variantsnssv790144
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557888
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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