A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560221



Internal ID16347630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112557960..112574905hg38UCSC Ensembl
Innerchr12:112995764..113012709hg19UCSC Ensembl
Innerchr12:111480147..111497092hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3816946
hg1916946
hg1816946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2875n54
Supporting Variantsnssv802339, nssv802338
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560221
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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