A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697535



Internal ID18995816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85657341..85762508hg38UCSC Ensembl
Innerchr9:88272256..88377423hg19UCSC Ensembl
Innerchr9:87462076..87567243hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38105168
hg19105168
hg18105168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051546
Supporting Variants
Samples
Known GenesAGTPBP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697535
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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