A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052372



Internal ID19141591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115722735..115734021hg38UCSC Ensembl
Innerchr12:116160540..116171826hg19UCSC Ensembl
Innerchr12:114644923..114656209hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3811287
hg1911287
hg1811287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1559n100
Supporting Variantsnssv3524955
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052372
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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