A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1534n100



Internal ID22787621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:83219138..83281121hg38UCSC Ensembl
chr12:83612917..83674900hg19UCSC Ensembl
chr12:82137048..82199031hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3861984
hg1961984
hg1861984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043439, nsv1050466
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)dgv1534n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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