A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv202n100



Internal ID22786289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79075272..79156017hg38UCSC Ensembl
chr1:79540957..79621702hg19UCSC Ensembl
chr1:79313545..79394290hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3880746
hg1980746
hg1880746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007013, nsv1009913, nsv1005743
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)dgv202n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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