A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv441n100



Internal ID20152057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157234232..157407788hg38UCSC Ensembl
chr1:157204022..157377578hg19UCSC Ensembl
chr1:155470646..155644202hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38173557
hg19173557
hg18173557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003039, nsv997549, nsv999712, nsv1011943
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)dgv441n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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