A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3431n100



Internal ID22789518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12387780..12434058hg38UCSC Ensembl
chr19:12498594..12544872hg19UCSC Ensembl
chr19:12359594..12405872hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3846279
hg1946279
hg1846279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058141, nsv1061424
Samples
Known GenesZNF443, ZNF799
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3431n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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