A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7390n100



Internal ID20159006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6656619..6745551hg38UCSC Ensembl
chr9:6656619..6745551hg19UCSC Ensembl
chr9:6646619..6735551hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3888933
hg1988933
hg1888933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028863, nsv1034003
Samples
Known GenesKDM4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7390n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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