A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv800699



Internal ID16094655
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 StatusS
Merged Variantsnsv559772
Supporting Variants
Samples
Known GenesLOC643339
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv800699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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