A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557801



Internal ID16345210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25803683..25805759hg38UCSC Ensembl
Innerchr12:25956617..25958693hg19UCSC Ensembl
Innerchr12:25847884..25849960hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382077
hg192077
hg182077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2416n54
Supporting Variantsnssv789871
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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