A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789875



Internal ID15737145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27064544..27217378hg38UCSC Ensembl
Innerchr12:27217477..27370311hg19UCSC Ensembl
Innerchr12:27108744..27261578hg18UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38152835
hg19152835
hg18152835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557805
Supporting Variants
Samples
Known GenesC12orf71
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv789875
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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