A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557754



Internal ID15998477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21898155..21919323hg38UCSC Ensembl
Innerchr12:22051089..22072257hg19UCSC Ensembl
Innerchr12:21942356..21963524hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3821169
hg1921169
hg1821169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv789580
Samples
Known GenesABCC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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