A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2770n100



Internal ID20154386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15031584..15100193hg38UCSC Ensembl
chr16:15125441..15194050hg19UCSC Ensembl
chr16:15032942..15101551hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3868610
hg1968610
hg1868610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054221, nsv1045158
Samples
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2770n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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