A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559805



Internal ID16347214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:94844280..94883604hg38UCSC Ensembl
Innerchr12:95238056..95277380hg19UCSC Ensembl
Innerchr12:93762187..93801511hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3839325
hg1939325
hg1839325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800746
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559805
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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