A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2874n100



Internal ID22788961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32384286..33644789hg38UCSC Ensembl
chr16:32395607..33447256hg19UCSC Ensembl
chr16:32303108..33354757hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381260504
hg191051650
hg181051650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057489, nsv1065547, nsv1066576, nsv1063636, nsv1058230
Samples
Known GenesLOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2874n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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