A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560436



Internal ID16001159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:120259667..120268025hg38UCSC Ensembl
Innerchr12:120697470..120705828hg19UCSC Ensembl
Innerchr12:119181853..119190211hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg388359
hg198359
hg188359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803396, nssv803397
Samples
Known GenesPXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560436
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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