A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038488



Internal ID19127707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:3312274..3341184hg38UCSC Ensembl
Innerchr12:3421440..3450350hg19UCSC Ensembl
Innerchr12:3291701..3320611hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3828911
hg1928911
hg1828911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510131
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)nsv1038488
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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