A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv800011



Internal ID16093967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:87053980..87115664hg38UCSC Ensembl
Innerchr12:87447757..87509441hg19UCSC Ensembl
Innerchr12:85971888..86033572hg18UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg3861685
hg1961685
hg1861685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559700
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)nssv800011
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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