A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7514n100



Internal ID22793601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32087211..32211780hg38UCSC Ensembl
chr9:32087209..32211778hg19UCSC Ensembl
chr9:32077209..32201778hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38124570
hg19124570
hg18124570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022632, nsv1024866
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)dgv7514n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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