A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035633



Internal ID18778164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69381047..69562068hg38UCSC Ensembl
Innerchr9:71995963..72176984hg19UCSC Ensembl
Innerchr9:71185783..71366804hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38181022
hg19181022
hg18181022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7668n100
Supporting Variantsnssv3696227
Samples
Known GenesAPBA1, FAM189A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035633
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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