A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559772



Internal ID16347181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:93110612..93119320hg38UCSC Ensembl
Innerchr12:93504388..93513096hg19UCSC Ensembl
Innerchr12:92028519..92037227hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg388709
hg198709
hg188709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800700, nssv800699, nssv800701
Samples
Known GenesLOC643339
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559772
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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