A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv797865



Internal ID16091821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:70480946..70482249hg38UCSC Ensembl
Innerchr12:70874726..70876029hg19UCSC Ensembl
Innerchr12:69160993..69162296hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg381304
hg191304
hg181304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559268
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)nssv797865
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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