A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4919n100



Internal ID20156535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151776103..151841876hg38UCSC Ensembl
chr3:151493891..151559664hg19UCSC Ensembl
chr3:152976581..153042354hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3865774
hg1965774
hg1865774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002653, nsv999322
Samples
Known GenesAADAC, LOC201651, MIR548H2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4919n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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