A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7477n100



Internal ID22793564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23326891..23410598hg38UCSC Ensembl
chr9:23326889..23410596hg19UCSC Ensembl
chr9:23316889..23400596hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3883708
hg1983708
hg1883708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026141, nsv1018333, nsv1033136, nsv1034873
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)dgv7477n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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