A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv146n100



Internal ID22786233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34622883..34638878hg38UCSC Ensembl
chr1:35088484..35104479hg19UCSC Ensembl
chr1:34861071..34877066hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3815996
hg1915996
hg1815996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011406, nsv1008561, nsv997969, nsv1002546, nsv1003697, nsv1001313
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)dgv146n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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