A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3132n100



Internal ID22789219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22288429..22736323hg38UCSC Ensembl
chr17:21815035..22235650hg19UCSC Ensembl
chr17:21739162..22159777hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38447895
hg19420616
hg18420616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065987, nsv1057019, nsv1066648, nsv1059086, nsv1058610, nsv1064766
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)dgv3132n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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