A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7702n100



Internal ID20159318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112761646..112790772hg38UCSC Ensembl
chr9:115523926..115553052hg19UCSC Ensembl
chr9:114563747..114592873hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3829127
hg1929127
hg1829127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045953, nsv1048733
Samples
Known GenesSNX30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7702n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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