A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7466n100



Internal ID22793553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17577143..17636676hg38UCSC Ensembl
chr9:17577141..17636674hg19UCSC Ensembl
chr9:17567141..17626674hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3859534
hg1959534
hg1859534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022691, nsv1032604, nsv1030902, nsv1029253, nsv1015810, nsv1017917, nsv1024129, nsv1021448, nsv1031193, nsv1019764, nsv1025072, nsv1033807
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7466n100
Frequency
Sample Size11257
Observed Gain29
Observed Loss0
Observed Complex0
Frequencyn/a


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