A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696227



Internal ID18994508
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 StatusS
Merged Variantsnsv1035633
Supporting Variants
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)nssv3696227
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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