A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3095n100



Internal ID20154711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6872614..6962694hg38UCSC Ensembl
chr17:6775933..6866013hg19UCSC Ensembl
chr17:6716657..6806737hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3890081
hg1990081
hg1890081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056795, nsv1062854, nsv1066556
Samples
Known GenesALOX12P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3095n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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