A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2762n100



Internal ID20154378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14954899..15022388hg38UCSC Ensembl
chr16:15048756..15116245hg19UCSC Ensembl
chr16:14956257..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3867490
hg1967490
hg1867490
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041009, nsv1045830, nsv1039303, nsv1040538
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2762n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss88
Observed Complex0
Frequencyn/a


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