A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5608n100



Internal ID22791695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26213048..26292706hg38UCSC Ensembl
chr5:26213157..26292815hg19UCSC Ensembl
chr5:26248914..26328572hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3879659
hg1979659
hg1879659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031254, nsv1030215
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)dgv5608n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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