A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3076n100



Internal ID22789163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:828833..920583hg38UCSC Ensembl
chr17:732073..823823hg19UCSC Ensembl
chr17:678823..770573hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3891751
hg1991751
hg1891751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060103, nsv1065162
Samples
Known GenesNXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3076n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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