A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019149



Internal ID18761683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33143183..33259779hg38UCSC Ensembl
Innerchr9:33143181..33259777hg19UCSC Ensembl
Innerchr9:33133181..33249777hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38116597
hg19116597
hg18116597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7516n100
Supporting Variantsnssv3688872
Samples
Known GenesB4GALT1, BAG1, LOC101929639, SPINK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019149
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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