A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3128n100



Internal ID20154744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21609743..22736323hg38UCSC Ensembl
chr17:21513010..22235650hg19UCSC Ensembl
chr17:21453603..22159777hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381126581
hg19722641
hg18706175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059283, nsv1064237, nsv1059278, nsv1058112
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3128n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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