A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7387n100



Internal ID20159003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6308178..6408875hg38UCSC Ensembl
chr9:6308178..6408875hg19UCSC Ensembl
chr9:6298178..6398875hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38100698
hg19100698
hg18100698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019222, nsv1024324
Samples
Known GenesTPD52L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7387n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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