A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039899



Internal ID19129118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90127989..90199200hg38UCSC Ensembl
Innerchr12:90521766..90592977hg19UCSC Ensembl
Innerchr12:89045897..89117108hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3871212
hg1971212
hg1871212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712586
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)nsv1039899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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