A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560437



Internal ID16001160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:120365980..120371787hg38UCSC Ensembl
Innerchr12:120803783..120809590hg19UCSC Ensembl
Innerchr12:119288166..119293973hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg385808
hg195808
hg185808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803398
Samples
Known GenesMSI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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