A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3605n100



Internal ID22789692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44390001..44434604hg38UCSC Ensembl
chr19:44894164..44938779hg19UCSC Ensembl
chr19:49586004..49630619hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3844604
hg1944616
hg1844616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065703, nsv1065783, nsv1058295, nsv1065424, nsv1055870, nsv1059267, nsv1063780
Samples
Known GenesZNF229, ZNF285
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3605n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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