A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3687n100



Internal ID20155303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58473466..58586475hg38UCSC Ensembl
chr19:58984833..59097842hg19UCSC Ensembl
chr19:63676645..63789654hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38113010
hg19113010
hg18113010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063835, nsv1056050
Samples
Known GenesCENPBD1P1, CHMP2A, LOC100131691, MIR6807, MZF1, SLC27A5, TRIM28, UBE2M, ZBTB45, ZNF324, ZNF446
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3687n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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