A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3079n100



Internal ID22789166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:860866..1067857hg38UCSC Ensembl
chr17:764106..971097hg19UCSC Ensembl
chr17:710856..917847hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38206992
hg19206992
hg18206992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060388, nsv1063078, nsv1056579, nsv1062530, nsv1061726
Samples
Known GenesABR, MIR3183, NXN, TIMM22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3079n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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