A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5325n100



Internal ID22791412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77259955..77334274hg38UCSC Ensembl
chr4:78181108..78255427hg19UCSC Ensembl
chr4:78400132..78474451hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3874320
hg1974320
hg1874320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003399, nsv1009375, nsv1003935, nsv1003000
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5325n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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