A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3090n100



Internal ID22789177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6188534..6232721hg38UCSC Ensembl
chr17:6091854..6136041hg19UCSC Ensembl
chr17:6032578..6076765hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3844188
hg1944188
hg1844188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062102, nsv1059023, nsv1064263, nsv1066096, nsv1063417, nsv1058345
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)dgv3090n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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