A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7411n100



Internal ID22793498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11459329..11631105hg38UCSC Ensembl
chr9:11459329..11631105hg19UCSC Ensembl
chr9:11449329..11621105hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38171777
hg19171777
hg18171777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020284, nsv1029341, nsv1016077
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7411n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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