A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5062n100



Internal ID20156678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21335..66815hg38UCSC Ensembl
chr4:21335..66707hg19UCSC Ensembl
chr4:11335..56707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3845481
hg1945373
hg1845373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009127, nsv1014322, nsv1009854, nsv1004981, nsv1011225, nsv999669, nsv1011030, nsv1004445
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)dgv5062n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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