A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5597n100



Internal ID22791684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19015972..19287336hg38UCSC Ensembl
chr5:19016081..19287445hg19UCSC Ensembl
chr5:19051838..19323202hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38271365
hg19271365
hg18271365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023692, nsv1032309, nsv1020930, nsv1028462
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)dgv5597n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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