A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044953



Internal ID18787484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84311899..84421258hg38UCSC Ensembl
Innerchr9:86926814..87036173hg19UCSC Ensembl
Innerchr9:86116634..86225993hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38109360
hg19109360
hg18109360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697530
Samples
Known GenesSLC28A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044953
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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