A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1510n100



Internal ID22787597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60611443..60701473hg38UCSC Ensembl
chr12:61005224..61095254hg19UCSC Ensembl
chr12:59291491..59381521hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3890031
hg1990031
hg1890031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049626, nsv1035259
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)dgv1510n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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