A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560545



Internal ID16001268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124524838..124541865hg38UCSC Ensembl
Innerchr12:125009384..125026411hg19UCSC Ensembl
Innerchr12:123575337..123592364hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3817028
hg1917028
hg1817028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803899
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560545
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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