A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5071n100



Internal ID20156687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66815..161923hg38UCSC Ensembl
chr4:66707..155713hg19UCSC Ensembl
chr4:56707..145713hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3895109
hg1989007
hg1889007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013359, nsv1008448, nsv1012102
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5071n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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