A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789870



Internal ID16083826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25803683..25805380hg38UCSC Ensembl
Innerchr12:25956617..25958314hg19UCSC Ensembl
Innerchr12:25847884..25849581hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381698
hg191698
hg181698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557800
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)nssv789870
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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