A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7468n100



Internal ID20159084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17739008..17919576hg38UCSC Ensembl
chr9:17739006..17919574hg19UCSC Ensembl
chr9:17729006..17909574hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38180569
hg19180569
hg18180569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023089, nsv1034673
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)dgv7468n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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