A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037527



Internal ID18780058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:18208543..18260193hg38UCSC Ensembl
Innerchr12:18361477..18413127hg19UCSC Ensembl
Innerchr12:18252744..18304394hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3851651
hg1951651
hg1851651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505068
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)nsv1037527
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