A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5475n100



Internal ID22791562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171484847..171585385hg38UCSC Ensembl
chr4:172405998..172506536hg19UCSC Ensembl
chr4:172642573..172743111hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38100539
hg19100539
hg18100539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026605, nsv1020112, nsv1034055, nsv1016311
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)dgv5475n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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