A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3109n100



Internal ID22789196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17404695..17445234hg38UCSC Ensembl
chr17:17308009..17348548hg19UCSC Ensembl
chr17:17248734..17289273hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3840540
hg1940540
hg1840540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058849, nsv1058804
Samples
Known GenesSMCR9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3109n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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