A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3607n100



Internal ID22789694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46190144..46279349hg38UCSC Ensembl
chr19:46693401..46782606hg19UCSC Ensembl
chr19:51385241..51474446hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3889206
hg1989206
hg1889206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066617, nsv1057897, nsv1063837
Samples
Known GenesDKFZp434J0226, IGFL1, RNU6-66P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3607n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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