A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1509n100



Internal ID22787596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:59875368..59909042hg38UCSC Ensembl
chr12:60269149..60302823hg19UCSC Ensembl
chr12:58555416..58589090hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3833675
hg1933675
hg1833675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055021, nsv1050201
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)dgv1509n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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