A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559156



Internal ID16346565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:62499419..62565357hg38UCSC Ensembl
Innerchr12:62893199..62959137hg19UCSC Ensembl
Innerchr12:61179466..61245404hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3865939
hg1965939
hg1865939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175476
Samples1780862194_A
Known GenesMON2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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