A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5074n100



Internal ID20156690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141044..286102hg38UCSC Ensembl
chr4:134825..279891hg19UCSC Ensembl
chr4:124825..269891hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38145059
hg19145067
hg18145067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005874, nsv1001793
Samples
Known GenesZNF718, ZNF732, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5074n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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