A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5077n100



Internal ID22791164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:355495..453210hg38UCSC Ensembl
chr4:349284..446999hg19UCSC Ensembl
chr4:339284..436999hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3897716
hg1997716
hg1897716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012409, nsv1003360, nsv997300
Samples
Known GenesABCA11P, ZNF141, ZNF721
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5077n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer