A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044897



Internal ID18787428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89756671..89943559hg38UCSC Ensembl
Innerchr12:90150448..90337336hg19UCSC Ensembl
Innerchr12:88674579..88861467hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38186889
hg19186889
hg18186889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524806
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)nsv1044897
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer