A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560555



Internal ID16001278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540246..124545024hg38UCSC Ensembl
Innerchr12:125024792..125029570hg19UCSC Ensembl
Innerchr12:123590745..123595523hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384779
hg194779
hg184779
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2940n54
Supporting Variantsnssv803957, nssv803959, nssv803958, nssv803960
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560555
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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