A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3429n100



Internal ID19013797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11911596..11950569hg38UCSC Ensembl
chr19:12022411..12061384hg19UCSC Ensembl
chr19:11883411..11922384hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3838974
hg1938974
hg1838974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057367, nsv1055297
Samples
Known GenesZNF69, ZNF700
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3429n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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