A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7600n100



Internal ID22793687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61520009..61627300hg38UCSC Ensembl
chr9:44727847..44835138hg19UCSC Ensembl
chr9:44667843..44775134hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38107292
hg19107292
hg18107292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016101, nsv1031249
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)dgv7600n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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