A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7676n100



Internal ID20159292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69492925..69503518hg38UCSC Ensembl
chr9:72107841..72118434hg19UCSC Ensembl
chr9:71297661..71308254hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3810594
hg1910594
hg1810594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047108, nsv1036231
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7676n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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