A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv549n100



Internal ID22786636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:196829423..196847588hg38UCSC Ensembl
chr1:196798553..196816718hg19UCSC Ensembl
chr1:195065176..195083341hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3818166
hg1918166
hg1818166
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999209, nsv1011846
Samples
Known GenesCFHR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv549n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss5
Observed Complex0
Frequencyn/a


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