A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560577



Internal ID16001300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540561..124541057hg38UCSC Ensembl
Innerchr12:125025107..125025603hg19UCSC Ensembl
Innerchr12:123591060..123591556hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38497
hg19497
hg18497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2943n54
Supporting Variantsnssv804114, nssv804113, nssv804112
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560577
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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