A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5559n100



Internal ID22791646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7167547..7210514hg38UCSC Ensembl
chr5:7167660..7210627hg19UCSC Ensembl
chr5:7220660..7263627hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3842968
hg1942968
hg1842968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031777, nsv1025665, nsv1017855, nsv1031129, nsv1024067
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)dgv5559n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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