A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3086n100



Internal ID22789173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4101015..4199530hg38UCSC Ensembl
chr17:4004309..4102825hg19UCSC Ensembl
chr17:3951058..4049574hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3898516
hg1998517
hg1898517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066507, nsv1061747, nsv1062699, nsv1064991
Samples
Known GenesANKFY1, CYB5D2, ZZEF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3086n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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