A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2728n100



Internal ID19013096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11333115..11449038hg38UCSC Ensembl
chr16:11426972..11542894hg19UCSC Ensembl
chr16:11334473..11450395hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38115924
hg19115923
hg18115923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050309, nsv1048116
Samples
Known GenesRMI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2728n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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