A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696229



Internal ID18647824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69413542..69564931hg38UCSC Ensembl
Innerchr9:72028458..72179847hg19UCSC Ensembl
Innerchr9:71218278..71369667hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38151390
hg19151390
hg18151390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048650
Supporting Variants
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)nssv3696229
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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