A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv232n100



Internal ID22786319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104561736..104633369hg38UCSC Ensembl
chr1:105104358..105175991hg19UCSC Ensembl
chr1:104905881..104977514hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3871634
hg1971634
hg1871634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013052, nsv999490, nsv1004836
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)dgv232n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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