A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5751n100



Internal ID22791838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103145965..103204665hg38UCSC Ensembl
chr5:102481669..102540366hg19UCSC Ensembl
chr5:102509568..102568265hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3858701
hg1958698
hg1858698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020598, nsv1032141, nsv1029568, nsv1029715, nsv1022720
Samples
Known GenesPPIP5K2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5751n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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