A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5065n100



Internal ID20156681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29013..256048hg38UCSC Ensembl
chr4:29013..249837hg19UCSC Ensembl
chr4:19013..239837hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38227036
hg19220825
hg18220825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003992, nsv1006518, nsv1008284, nsv1000788
Samples
Known GenesZNF595, ZNF718, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5065n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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