A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3032n100



Internal ID22789119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77984145..78046521hg38UCSC Ensembl
chr16:78018042..78080418hg19UCSC Ensembl
chr16:76575543..76637919hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3862377
hg1962377
hg1862377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062975, nsv1064582, nsv1056127
Samples
Known GenesCLEC3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3032n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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