A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7461n100



Internal ID22793548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15841109..15880387hg38UCSC Ensembl
chr9:15841107..15880385hg19UCSC Ensembl
chr9:15831107..15870385hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3839279
hg1939279
hg1839279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032081, nsv1016226, nsv1027790, nsv1015435
Samples
Known GenesCCDC171
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7461n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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