A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7599n100



Internal ID22793686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61520009..61598565hg38UCSC Ensembl
chr9:44727847..44806403hg19UCSC Ensembl
chr9:44667843..44746399hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3878557
hg1978557
hg1878557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023151, nsv1023666
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)dgv7599n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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