A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7718n100



Internal ID19018086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130496996..130619919hg38UCSC Ensembl
chr9:133372383..133495306hg19UCSC Ensembl
chr9:132362204..132485127hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38122924
hg19122924
hg18122924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052423, nsv1036145
Samples
Known GenesASS1, FUBP3, LOC100272217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7718n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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