A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv201n100



Internal ID22786288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78838065..78879245hg38UCSC Ensembl
chr1:79303750..79344930hg19UCSC Ensembl
chr1:79076338..79117518hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3841181
hg1941181
hg1841181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003295, nsv1000656
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)dgv201n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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