A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv790889



Internal ID16084845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30080965..30089944hg38UCSC Ensembl
Innerchr12:30233898..30242877hg19UCSC Ensembl
Innerchr12:30125165..30134144hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg388980
hg198980
hg188980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557984
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv790889
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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